Linked Data
ClinVar Variation Id:
498519
dbSNP Id:
rs56174879
ExAC:
8:38277237 C / T
gnomAD v2:
8-38277237-C-T
gnomAD v3:
8-38419719-C-T
gnomAD v4:
8-38419719-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38419719C>T , CM000670.2:g.38419719C>T | GRCh38 |
| NC_000008.10:g.38277237C>T , CM000670.1:g.38277237C>T | GRCh37 |
| NC_000008.9:g.38396394C>T | NCBI36 |
| NG_007729.1:g.54116G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703405.1:c.1098G>A | ENSP00000515291.1:p.Pro366= | |
| ENST00000341462.9:c.1092G>A | ENSP00000340636.7:p.Pro364= | |
| ENST00000425967.8:c.1092G>A | ENSP00000393312.4:p.Pro364= | |
| ENST00000524528.2:n.832G>A | ||
| ENST00000683765.1:c.1284G>A | ENSP00000507039.1:p.Pro428= | |
| ENST00000683815.1:c.1092G>A | ENSP00000507997.1:p.Pro364= | |
| ENST00000683948.1:n.1792G>A | ||
| ENST00000684654.1:c.825G>A | ENSP00000507205.1:p.Pro275= | |
| ENST00000447712.7:c.1098G>A MANE Select | ENSP00000400162.2:p.Pro366= | |
| ENST00000649678.1:c.1092G>A | ENSP00000497266.1:p.Pro364= | |
| ENST00000674189.1:c.*750G>A | ENSP00000501345.1:n.*750G>A | |
| ENST00000674217.1:n.1605G>A | ||
| ENST00000674235.1:c.885G>A | ||
| ENST00000674380.1:c.*1065G>A | ENSP00000501514.1:n.*1065G>A | |
| ENST00000674474.1:n.2592G>A | ||
| ENST00000326324.10:c.825G>A | ENSP00000327229.6:p.Pro275= | |
| ENST00000335922.9:c.1074G>A | ENSP00000337247.5:p.Pro358= | |
| ENST00000341462.8:c.*148G>A | ENSP00000340636.6:n.*148G>A | |
| ENST00000356207.9:c.831G>A | ENSP00000348537.5:p.Pro277= | |
| ENST00000397091.9:c.1092G>A | ENSP00000380280.5:p.Pro364= | |
| ENST00000397103.5:c.831G>A | ENSP00000380292.1:p.Pro277= | |
| ENST00000397108.8:c.1092G>A | ENSP00000380297.4:p.Pro364= | |
| ENST00000397113.6:c.1092G>A | ENSP00000380302.2:p.Pro364= | |
| ENST00000425967.7:c.1191G>A | ENSP00000393312.3:p.Pro397= | |
| ENST00000447712.6:c.1098G>A | ENSP00000400162.2:p.Pro366= | |
| ENST00000466021.5:n.265G>A | ||
| ENST00000487647.5:c.975G>A | ENSP00000435254.1:n.975G>A | |
| ENST00000526570.5:n.3377G>A | ||
| ENST00000527114.5:n.626G>A | ||
| ENST00000527745.3:n.326G>A | ||
| ENST00000532791.5:c.1098G>A | ENSP00000432972.1:p.Pro366= | |
| ENST00000619564.3:c.680G>A | ENSP00000484553.1:p.Arg227Gln | |
| NM_001174063.1:c.1098G>A | NP_001167534.1:p.Pro366= | |
| NM_001174064.1:c.1074G>A | NP_001167535.1:p.Pro358= | |
| NM_001174065.1:c.1092G>A | NP_001167536.1:p.Pro364= | |
| NM_001174066.1:c.831G>A | NP_001167537.1:p.Pro277= | |
| NM_001174067.1:c.1191G>A | NP_001167538.1:p.Pro397= | |
| NM_015850.3:c.1092G>A | NP_056934.2:p.Pro364= | |
| NM_023105.2:c.831G>A | NP_075593.1:p.Pro277= | |
| NM_023106.2:c.825G>A | NP_075594.1:p.Pro275= | |
| NM_023110.2:c.1098G>A | NP_075598.2:p.Pro366= | |
| XM_006716303.2:c.1098G>A | XP_006716366.1:p.Pro366= | |
| XM_006716304.1:c.1098G>A | XP_006716367.1:p.Pro366= | |
| XM_006716305.2:c.1098G>A | XP_006716368.1:p.Pro366= | |
| XM_006716306.2:c.1092G>A | XP_006716369.1:p.Pro364= | |
| XM_006716307.1:c.1092G>A | XP_006716370.1:p.Pro364= | |
| XM_006716309.2:c.1074G>A | XP_006716372.1:p.Pro358= | |
| XM_006716310.2:c.831G>A | XP_006716373.1:p.Pro277= | |
| XM_006716311.1:c.831G>A | XP_006716374.1:p.Pro277= | |
| XM_006716312.1:c.831G>A | XP_006716375.1:p.Pro277= | |
| XM_006716313.2:c.825G>A | XP_006716376.1:p.Pro275= | |
| XM_006716314.1:c.825G>A | XP_006716377.1:p.Pro275= | |
| XM_011544443.1:c.1197G>A | XP_011542745.1:p.Pro399= | |
| XM_011544444.1:c.1191G>A | XP_011542746.1:p.Pro397= | |
| XM_011544445.1:c.1197G>A | XP_011542747.1:p.Pro399= | |
| XM_011544446.1:c.1197G>A | XP_011542748.1:p.Pro399= | |
| XM_011544447.1:c.1197G>A | XP_011542749.1:p.Pro399= | |
| XM_011544448.1:c.930G>A | XP_011542750.1:p.Pro310= | |
| XM_011544449.1:c.924G>A | XP_011542751.1:p.Pro308= | |
| XM_011544450.1:c.924G>A | XP_011542752.1:p.Pro308= | |
| XM_011544451.1:c.807G>A | XP_011542753.1:p.Pro269= | |
| NM_001354367.1:c.1092G>A | NP_001341296.1:p.Pro364= | |
| NM_001354368.1:c.825G>A | NP_001341297.1:p.Pro275= | |
| NM_001354369.1:c.1092G>A | NP_001341298.1:p.Pro364= | |
| NM_001354370.1:c.825G>A | NP_001341299.1:p.Pro275= | |
| XM_006716303.3:c.1098G>A | XP_006716366.1:p.Pro366= | |
| XM_006716310.3:c.831G>A | XP_006716373.1:p.Pro277= | |
| XM_006716312.2:c.831G>A | XP_006716375.1:p.Pro277= | |
| XM_006716314.2:c.825G>A | XP_006716377.1:p.Pro275= | |
| XM_011544443.2:c.1197G>A | XP_011542745.1:p.Pro399= | |
| XM_011544445.2:c.1197G>A | XP_011542747.1:p.Pro399= | |
| XM_011544446.2:c.1197G>A | XP_011542748.1:p.Pro399= | |
| XM_011544447.2:c.1197G>A | XP_011542749.1:p.Pro399= | |
| XM_011544450.2:c.924G>A | XP_011542752.1:p.Pro308= | |
| XM_017013219.1:c.1191G>A | XP_016868708.1:p.Pro397= | |
| XM_017013220.1:c.1191G>A | XP_016868709.1:p.Pro397= | |
| XM_017013221.1:c.1098G>A | XP_016868710.1:p.Pro366= | |
| XM_017013222.2:c.1098G>A | XP_016868711.1:p.Pro366= | |
| XM_017013224.2:c.1092G>A | XP_016868713.1:p.Pro364= | |
| XM_017013225.2:c.1092G>A | XP_016868714.1:p.Pro364= | |
| XM_017013226.1:c.930G>A | XP_016868715.1:p.Pro310= | |
| XM_017013227.1:c.924G>A | XP_016868716.1:p.Pro308= | |
| XM_017013229.2:c.132G>A | XP_016868718.1:p.Pro44= | |
| XM_017013230.1:c.132G>A | XP_016868719.1:p.Pro44= | |
| XM_024447097.1:c.1074G>A | XP_024302865.1:p.Pro358= | |
| XR_001745495.1:n.1346G>A | ||
| XR_001745496.1:n.1346G>A | ||
| NM_001174063.2:c.1098G>A | NP_001167534.1:p.Pro366= | |
| NM_001174064.2:c.1074G>A | NP_001167535.1:p.Pro358= | |
| NM_001174065.2:c.1092G>A | NP_001167536.1:p.Pro364= | |
| NM_001174066.2:c.831G>A | NP_001167537.1:p.Pro277= | |
| NM_001354368.2:c.825G>A | NP_001341297.1:p.Pro275= | |
| NM_015850.4:c.1092G>A | NP_056934.2:p.Pro364= | |
| NM_023105.3:c.831G>A | NP_075593.1:p.Pro277= | |
| NM_023106.3:c.825G>A | NP_075594.1:p.Pro275= | |
| NM_023110.3:c.1098G>A MANE Select | NP_075598.2:p.Pro366= | |
| NM_001174067.2:c.1191G>A | NP_001167538.1:p.Pro397= | |
| NM_001354367.2:c.1092G>A | NP_001341296.1:p.Pro364= | |
| NM_001354369.2:c.1092G>A | NP_001341298.1:p.Pro364= | |
| NM_001354370.2:c.825G>A | NP_001341299.1:p.Pro275= |