Linked Data
ClinVar Variation Id:
499552
dbSNP Id:
rs760263014
ExAC:
12:49433982 G / A
gnomAD v2:
12-49433982-G-A
gnomAD v3:
12-49040199-G-A
gnomAD v4:
12-49040199-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49040199G>A , CM000674.2:g.49040199G>A | GRCh38 |
| NC_000012.11:g.49433982G>A , CM000674.1:g.49433982G>A | GRCh37 |
| NC_000012.10:g.47720249G>A | NCBI36 |
| NG_027827.1:g.20126C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683543.2:c.7571C>T | ENSP00000506726.1:p.Thr2524Met | |
| ENST00000685166.1:c.7580C>T | ENSP00000509386.1:p.Thr2527Met | |
| ENST00000689060.1:c.1590C>T | ||
| ENST00000689143.1:c.1244C>T | ENSP00000509839.1:p.Thr415Met | |
| ENST00000689944.1:c.1680C>T | ||
| ENST00000692637.1:c.7568C>T | ENSP00000509666.1:p.Thr2523Met | |
| ENST00000301067.12:c.7571C>T MANE Select | ENSP00000301067.7:p.Thr2524Met | |
| ENST00000301067.11:c.7571C>T | ENSP00000301067.7:p.Thr2524Met | |
| NM_003482.3:c.7571C>T | NP_003473.3:p.Thr2524Met | |
| XM_005269162.3:c.7571C>T | XP_005269219.1:p.Thr2524Met | |
| XM_006719614.2:c.7580C>T | XP_006719677.1:p.Thr2527Met | |
| XM_006719616.2:c.7568C>T | XP_006719679.1:p.Thr2523Met | |
| XM_011538770.1:c.7580C>T | XP_011537072.1:p.Thr2527Met | |
| XM_011538771.1:c.7577C>T | XP_011537073.1:p.Thr2526Met | |
| XM_011538772.1:c.7571C>T | XP_011537074.1:p.Thr2524Met | |
| XM_011538773.1:c.7568C>T | XP_011537075.1:p.Thr2523Met | |
| XM_011538774.1:c.7559C>T | XP_011537076.1:p.Thr2520Met | |
| XM_011538775.1:c.7580C>T | XP_011537077.1:p.Thr2527Met | |
| XM_011538776.1:c.7487C>T | XP_011537078.1:p.Thr2496Met | |
| XR_944740.1:n.9900C>T | ||
| XM_005269162.4:c.7571C>T | XP_005269219.1:p.Thr2524Met | |
| XM_006719614.4:c.7580C>T | XP_006719677.1:p.Thr2527Met | |
| XM_006719616.3:c.7568C>T | XP_006719679.1:p.Thr2523Met | |
| XM_011538770.2:c.7580C>T | XP_011537072.1:p.Thr2527Met | |
| XM_011538771.2:c.7577C>T | XP_011537073.1:p.Thr2526Met | |
| XM_011538772.2:c.7571C>T | XP_011537074.1:p.Thr2524Met | |
| XM_011538773.2:c.7568C>T | XP_011537075.1:p.Thr2523Met | |
| XM_011538774.2:c.7559C>T | XP_011537076.1:p.Thr2520Met | |
| XM_011538776.2:c.7487C>T | XP_011537078.1:p.Thr2496Met | |
| XR_001748874.1:n.8889C>T | ||
| NM_003482.4:c.7571C>T MANE Select | NP_003473.3:p.Thr2524Met |