Linked Data
ClinVar Variation Id:
413534
dbSNP Id:
rs574033788
ExAC:
12:133248814 G / A
gnomAD v2:
12-133248814-G-A
gnomAD v3:
12-132672228-G-A
gnomAD v4:
12-132672228-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.132672228G>A , CM000674.2:g.132672228G>A | GRCh38 |
| NC_000012.11:g.133248814G>A , CM000674.1:g.133248814G>A | GRCh37 |
| NC_000012.10:g.131758887G>A | NCBI36 |
| NG_033840.1:g.20297C>T , LRG_789:g.20297C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000539215.6:c.536C>T | ||
| ENST00000699982.1:c.1635C>T | ||
| ENST00000699983.1:c.1635C>T | ||
| ENST00000699984.1:c.1635C>T | ||
| ENST00000320574.10:c.1781C>T MANE Select | ENSP00000322570.5:p.Thr594Ile | |
| ENST00000672742.1:c.*1283C>T | ENSP00000500279.1:n.*1283C>T | |
| ENST00000320574.9:c.1781C>T | ENSP00000322570.5:p.Thr594Ile | |
| ENST00000535270.5:c.1700C>T | ENSP00000445753.1:p.Thr567Ile | |
| ENST00000537064.5:c.*828C>T | ENSP00000442578.1:n.*828C>T | |
| NM_006231.3:c.1781C>T , LRG_789t1:c.1781C>T | NP_006222.2:p.Thr594Ile | |
| XM_011534795.1:c.1781C>T | XP_011533097.1:p.Thr594Ile | |
| XM_011534796.1:c.1652C>T | XP_011533098.1:p.Thr551Ile | |
| XM_011534797.1:c.860C>T | XP_011533099.1:p.Thr287Ile | |
| XM_011534798.1:c.443C>T | XP_011533100.1:p.Thr148Ile | |
| XM_011534799.1:c.1781C>T | XP_011533101.1:p.Thr594Ile | |
| XM_011534800.1:c.1781C>T | XP_011533102.1:p.Thr594Ile | |
| XM_011534801.1:c.1781C>T | XP_011533103.1:p.Thr594Ile | |
| XR_941395.1:n.1990C>T | ||
| XM_011534795.3:c.1781C>T | XP_011533097.1:p.Thr594Ile | |
| XM_011534797.3:c.860C>T | XP_011533099.1:p.Thr287Ile | |
| XM_011534799.2:c.1781C>T | XP_011533101.1:p.Thr594Ile | |
| XR_002957338.1:n.1985C>T | ||
| XR_002957339.1:n.1985C>T | ||
| XR_941395.2:n.1985C>T | ||
| NM_006231.4:c.1781C>T MANE Select | NP_006222.2:p.Thr594Ile |