Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118110090A>T , CM000670.2:g.118110090A>T | GRCh38 |
| NC_000008.10:g.119122329A>T , CM000670.1:g.119122329A>T | GRCh37 |
| NC_000008.9:g.119191510A>T | NCBI36 |
| NG_007455.2:g.6730T>A , LRG_493:g.6730T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000127.3:c.957T>A MANE Select | NP_000118.2:p.Tyr319Ter |
| ENST00000378204.7:c.957T>A MANE Select | ENSP00000367446.3:p.Tyr319Ter |
| NM_000127.2:c.957T>A , LRG_493t1:c.957T>A | NP_000118.2:p.Tyr319Ter |
| ENST00000378204.6:c.957T>A | ENSP00000367446.2:p.Tyr319Ter |
| ENST00000436216.1:c.325T>A | |
| ENST00000436216.2:c.325T>A | |
| ENST00000437196.1:c.73+884T>A | ENSP00000407299.1:n.73+884T>A |