Linked Data
dbSNP Id:
rs373661257
gnomAD v2:
2-16085655-C-A
gnomAD v3:
2-15945533-C-A
gnomAD v4:
2-15945533-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.15945533C>A , CM000664.2:g.15945533C>A | GRCh38 |
| NC_000002.11:g.16085655C>A , CM000664.1:g.16085655C>A | GRCh37 |
| NC_000002.10:g.16003106C>A | NCBI36 |
| NG_007457.1:g.9973C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703162.1:n.180C>A | ||
| ENST00000281043.4:c.831C>A MANE Select | ENSP00000281043.3:p.Ile277= | |
| ENST00000638417.1:c.198C>A | ENSP00000491476.1:p.Ile66= | |
| ENST00000281043.3:c.831C>A | ENSP00000281043.3:p.Ile277= | |
| NM_001293228.1:c.831C>A | NP_001280157.1:p.Ile277= | |
| NM_001293231.1:c.198C>A | NP_001280160.1:p.Ile66= | |
| NM_001293233.1:c.*766C>A | NP_001280162.1:n.*766C>A | |
| NM_005378.5:c.831C>A | NP_005369.2:p.Ile277= | |
| NM_005378.6:c.831C>A MANE Select | NP_005369.2:p.Ile277= | |
| NM_001293228.2:c.831C>A | NP_001280157.1:p.Ile277= | |
| NM_001293231.2:c.198C>A | NP_001280160.1:p.Ile66= | |
| NM_001293233.2:c.*766C>A | NP_001280162.1:n.*766C>A |