Linked Data
gnomAD v4:
6-151615606-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151615606T>C , CM000668.2:g.151615606T>C | GRCh38 |
| NC_000006.11:g.151936741T>C , CM000668.1:g.151936741T>C | GRCh37 |
| NC_000006.10:g.151978434T>C | NCBI36 |
| NG_021198.1:g.126567T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239374.8:c.1874T>C MANE Select | ENSP00000239374.6:p.Met625Thr | |
| ENST00000239374.7:c.1874T>C | ENSP00000239374.6:p.Met625Thr | |
| NM_025059.3:c.1874T>C | NP_079335.2:p.Met625Thr | |
| XM_011536147.1:c.1892T>C | XP_011534449.1:p.Met631Thr | |
| XM_011536148.1:c.1691T>C | XP_011534450.1:p.Met564Thr | |
| XM_011536147.2:c.1892T>C | XP_011534449.1:p.Met631Thr | |
| XM_011536148.2:c.1691T>C | XP_011534450.1:p.Met564Thr | |
| XR_001743865.1:n.129+1115A>G | ||
| NM_025059.4:c.1874T>C MANE Select | NP_079335.2:p.Met625Thr |