Linked Data
ClinVar Variation Id:
379061
dbSNP Id:
rs533565295
ExAC:
9:135772041 C / T
gnomAD v2:
9-135772041-C-T
gnomAD v4:
9-132896654-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.132896654C>T , CM000671.2:g.132896654C>T | GRCh38 |
| NC_000009.11:g.135772041C>T , CM000671.1:g.135772041C>T | GRCh37 |
| NC_000009.10:g.134761862C>T | NCBI36 |
| NG_012386.1:g.52980G>A , LRG_486:g.52980G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000475903.7:c.3073G>A | ENSP00000496126.2:p.Ala1025Thr | |
| ENST00000490179.4:c.3076G>A | ENSP00000495533.2:p.Ala1026Thr | |
| ENST00000642261.2:c.*932G>A | ENSP00000494743.2:n.*932G>A | |
| ENST00000643275.2:c.*1016G>A | ENSP00000495598.2:n.*1016G>A | |
| ENST00000643362.2:c.2689G>A | ENSP00000496398.2:p.Ala897Thr | |
| ENST00000643625.2:c.*818G>A | ENSP00000495546.2:n.*818G>A | |
| ENST00000643691.2:c.2713G>A | ENSP00000494916.2:p.Ala905Thr | |
| ENST00000644184.2:c.3034G>A | ENSP00000495428.2:p.Ala1012Thr | |
| ENST00000645129.2:c.2920G>A | ENSP00000493639.2:p.Ala974Thr | |
| ENST00000646440.2:c.3076G>A | ENSP00000495830.2:p.Ala1026Thr | |
| ENST00000298552.9:c.3076G>A MANE Select | ENSP00000298552.3:p.Ala1026Thr | |
| ENST00000642261.1:c.1213G>A | ||
| ENST00000642617.1:c.3073G>A | ENSP00000493773.1:p.Ala1025Thr | |
| ENST00000642627.1:c.3058G>A | ENSP00000496772.1:p.Ala1020Thr | |
| ENST00000642811.1:c.*2846G>A | ENSP00000495554.1:n.*2846G>A | |
| ENST00000643072.1:c.2923G>A | ENSP00000496691.1:p.Ala975Thr | |
| ENST00000643275.1:c.1550G>A | ENSP00000495598.1:n.1550G>A | |
| ENST00000643583.1:c.3061G>A | ENSP00000494685.1:p.Ala1021Thr | |
| ENST00000643625.1:c.953G>A | ENSP00000495546.1:n.953G>A | |
| ENST00000643875.1:c.3076G>A | ENSP00000495158.1:p.Ala1026Thr | |
| ENST00000644097.1:c.3073G>A | ENSP00000494682.1:p.Ala1025Thr | |
| ENST00000644184.1:c.1771G>A | ENSP00000495428.1:p.Ala591Thr | |
| ENST00000644255.1:c.*2843G>A | ENSP00000493608.1:n.*2843G>A | |
| ENST00000644319.1:n.3451G>A | ||
| ENST00000644786.1:n.735G>A | ||
| ENST00000644882.1:n.1984G>A | ||
| ENST00000645901.1:n.3927G>A | ||
| ENST00000646391.1:c.*2846G>A | ENSP00000494104.1:n.*2846G>A | |
| ENST00000646625.1:c.3076G>A | ENSP00000496263.1:p.Ala1026Thr | |
| ENST00000647262.1:n.2041G>A | ||
| ENST00000647279.1:c.*2315G>A | ENSP00000494502.1:n.*2315G>A | |
| ENST00000647534.1:n.2140G>A | ||
| ENST00000298552.7:c.3076G>A | ENSP00000298552.3:p.Ala1026Thr | |
| ENST00000440111.6:c.3076G>A | ENSP00000394524.2:p.Ala1026Thr | |
| ENST00000545250.5:c.2923G>A | ENSP00000444017.1:p.Ala975Thr | |
| NM_000368.4:c.3076G>A , LRG_486t1:c.3076G>A | NP_000359.1:p.Ala1026Thr | |
| NM_001162426.1:c.3073G>A | NP_001155898.1:p.Ala1025Thr | |
| NM_001162427.1:c.2923G>A | NP_001155899.1:p.Ala975Thr | |
| XM_005272211.1:c.3076G>A | XP_005272268.1:p.Ala1026Thr | |
| XM_006717271.1:c.3076G>A | XP_006717334.1:p.Ala1026Thr | |
| XM_011518979.1:c.3076G>A | XP_011517281.1:p.Ala1026Thr | |
| NM_001362177.1:c.2713G>A | NP_001349106.1:p.Ala905Thr | |
| XM_011518979.2:c.3076G>A | XP_011517281.1:p.Ala1026Thr | |
| XM_017015096.1:c.3076G>A | XP_016870585.1:p.Ala1026Thr | |
| XM_017015097.1:c.3076G>A | XP_016870586.1:p.Ala1026Thr | |
| XM_017015098.1:c.3073G>A | XP_016870587.1:p.Ala1025Thr | |
| XM_017015100.1:c.2713G>A | XP_016870589.1:p.Ala905Thr | |
| XM_017015101.1:c.2710G>A | XP_016870590.1:p.Ala904Thr | |
| NM_000368.5:c.3076G>A MANE Select | NP_000359.1:p.Ala1026Thr | |
| NM_001162426.2:c.3073G>A | NP_001155898.1:p.Ala1025Thr | |
| NM_001162427.2:c.2923G>A | NP_001155899.1:p.Ala975Thr | |
| NM_001362177.2:c.2713G>A | NP_001349106.1:p.Ala905Thr |