Linked Data
ClinVar Variation Id:
1472540
ClinVar RCV Id:
RCV002005031
dbSNP Id:
rs749261715
ExAC:
3:142281262 T / C
gnomAD v2:
3-142281262-T-C
gnomAD v4:
3-142562420-T-C
COSMIC:
COSM3125222
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.142562420T>C , CM000665.2:g.142562420T>C | GRCh38 |
| NC_000003.11:g.142281262T>C , CM000665.1:g.142281262T>C | GRCh37 |
| NC_000003.10:g.143763952T>C | NCBI36 |
| NG_008951.1:g.21407A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000350721.9:c.982A>G MANE Select | ENSP00000343741.4:p.Met328Val | |
| ENST00000515149.3:c.293-999A>G | ENSP00000425897.3:n.293-999A>G | |
| ENST00000653868.1:n.1011A>G | ||
| ENST00000657914.1:n.3340A>G | ||
| ENST00000659195.1:n.3047A>G | ||
| ENST00000661310.1:c.982A>G | ENSP00000499589.1:p.Met328Val | |
| ENST00000350721.8:c.982A>G | ENSP00000343741.4:p.Met328Val | |
| ENST00000507148.1:c.293-72A>G | ENSP00000426595.1:n.293-72A>G | |
| ENST00000515149.2:c.25A>G | ENSP00000425897.2:p.Met9Val | |
| NM_001184.3:c.982A>G | NP_001175.2:p.Met328Val | |
| XM_011512924.1:c.982A>G | XP_011511226.1:p.Met328Val | |
| XM_011512925.1:c.982A>G | XP_011511227.1:p.Met328Val | |
| XM_011512926.1:c.982A>G | XP_011511228.1:p.Met328Val | |
| XM_011512927.1:c.982A>G | XP_011511229.1:p.Met328Val | |
| XR_924147.1:n.1071A>G | ||
| XR_924148.1:n.1071A>G | ||
| XR_924149.1:n.1071A>G | ||
| NM_001354579.1:c.982A>G | NP_001341508.1:p.Met328Val | |
| XR_001740179.2:n.1071A>G | ||
| XR_001740180.2:n.1071A>G | ||
| XR_001740181.2:n.1071A>G | ||
| XR_001740182.1:n.1071A>G | ||
| XR_002959543.1:n.1071A>G | ||
| XR_924148.2:n.1071A>G | ||
| NM_001184.4:c.982A>G MANE Select | NP_001175.2:p.Met328Val | |
| NM_001354579.2:c.982A>G | NP_001341508.1:p.Met328Val |