Linked Data
ClinVar Variation Id:
156536
dbSNP Id:
rs587777851
gnomAD v4:
3-142541008-C-A
PubMed:
PMID:23144622
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.142541008C>A , CM000665.2:g.142541008C>A | GRCh38 |
| NC_000003.11:g.142259850C>A , CM000665.1:g.142259850C>A | GRCh37 |
| NC_000003.10:g.143742540C>A | NCBI36 |
| NG_008951.1:g.42819G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000350721.9:c.3477G>T MANE Select | ENSP00000343741.4:p.Met1159Ile | |
| ENST00000515149.3:c.*2251G>T | ENSP00000425897.3:n.*2251G>T | |
| ENST00000653868.1:n.3506G>T | ||
| ENST00000656582.1:n.736G>T | ||
| ENST00000656590.1:c.2267G>T | ||
| ENST00000661310.1:c.3285G>T | ENSP00000499589.1:p.Met1095Ile | |
| ENST00000350721.8:c.3477G>T | ENSP00000343741.4:p.Met1159Ile | |
| NM_001184.3:c.3477G>T | NP_001175.2:p.Met1159Ile | |
| XM_011512924.1:c.3477G>T | XP_011511226.1:p.Met1159Ile | |
| XM_011512925.1:c.3285G>T | XP_011511227.1:p.Met1095Ile | |
| XM_011512926.1:c.3477G>T | XP_011511228.1:p.Met1159Ile | |
| XM_011512927.1:c.3477G>T | XP_011511229.1:p.Met1159Ile | |
| XR_924147.1:n.3566G>T | ||
| XR_924148.1:n.3566G>T | ||
| XR_924149.1:n.3566G>T | ||
| NM_001354579.1:c.3285G>T | NP_001341508.1:p.Met1095Ile | |
| XR_001740179.2:n.3566G>T | ||
| XR_001740180.2:n.3566G>T | ||
| XR_001740181.2:n.3566G>T | ||
| XR_001740182.1:n.3566G>T | ||
| XR_002959543.1:n.3566G>T | ||
| XR_924148.2:n.3566G>T | ||
| NM_001184.4:c.3477G>T MANE Select | NP_001175.2:p.Met1159Ile | |
| NM_001354579.2:c.3285G>T | NP_001341508.1:p.Met1095Ile |