Linked Data
ClinVar Variation Id:
407246
ClinVar RCV Id:
RCV000477129
dbSNP Id:
rs749078502
ExAC:
5:13922370 G / A
gnomAD v2:
5-13922370-G-A
gnomAD v4:
5-13922261-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13922261G>A , CM000667.2:g.13922261G>A | GRCh38 |
| NC_000005.9:g.13922370G>A , CM000667.1:g.13922370G>A | GRCh37 |
| NC_000005.8:g.13975370G>A | NCBI36 |
| NG_013081.1:g.27220C>T | |
| NG_013081.2:g.27220C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680213.2:n.562C>T | ||
| ENST00000682376.1:n.550C>T | ||
| ENST00000682586.1:n.550C>T | ||
| ENST00000683011.1:n.445C>T | ||
| ENST00000683967.1:n.556C>T | ||
| ENST00000684013.1:n.556C>T | ||
| ENST00000684099.1:n.601C>T | ||
| ENST00000265104.5:c.506C>T MANE Select | ENSP00000265104.4:p.Ser169Leu | |
| ENST00000680213.1:c.266C>T | ENSP00000506622.1:p.Ser89Leu | |
| ENST00000681290.1:c.461C>T | ENSP00000505288.1:p.Ser154Leu | |
| ENST00000265104.4:c.506C>T | ENSP00000265104.4:p.Ser169Leu | |
| ENST00000508040.1:n.865C>T | ||
| NM_001369.2:c.506C>T | NP_001360.1:p.Ser169Leu | |
| XM_005248262.2:c.461C>T | XP_005248319.1:p.Ser154Leu | |
| XM_011513990.1:c.506C>T | XP_011512292.1:p.Ser169Leu | |
| XR_925598.1:n.713C>T | ||
| XM_005248262.3:c.614C>T | XP_005248319.2:p.Ser205Leu | |
| XM_017009177.1:c.614C>T | XP_016864666.1:p.Ser205Leu | |
| XM_017009178.1:c.-531C>T | XP_016864667.1:n.-531C>T | |
| XM_017009180.1:c.614C>T | XP_016864669.1:p.Ser205Leu | |
| XM_017009181.1:c.614C>T | XP_016864670.1:p.Ser205Leu | |
| XM_017009182.1:c.614C>T | XP_016864671.1:p.Ser205Leu | |
| XM_017009183.1:c.614C>T | XP_016864672.1:p.Ser205Leu | |
| XM_017009184.1:c.614C>T | XP_016864673.1:p.Ser205Leu | |
| XM_017009187.1:c.614C>T | XP_016864676.1:p.Ser205Leu | |
| XM_024454388.1:c.-2401C>T | XP_024310156.1:n.-2401C>T | |
| XM_024454389.1:c.-1454C>T | XP_024310157.1:n.-1454C>T | |
| XR_001742034.1:n.631C>T | ||
| XR_001742035.1:n.631C>T | ||
| NM_001369.3:c.506C>T MANE Select | NP_001360.1:p.Ser169Leu |