HGVS | Genome Assembly |
---|---|
NC_000001.11:g.1535669A>T , CM000663.2:g.1535669A>T | GRCh38 |
NC_000001.10:g.1471049A>T , CM000663.1:g.1471049A>T | GRCh37 |
NC_000001.9:g.1460912A>T | NCBI36 |
NG_041807.1:g.9692T>A | |
NG_053035.1:g.28527A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378733.9:c.293T>A MANE Select | ENSP00000368007.4:p.Phe98Tyr | |
ENST00000378733.8:c.293T>A | ENSP00000368007.4:p.Phe98Tyr | |
ENST00000425828.1:c.293T>A | ENSP00000400311.1:p.Phe98Tyr | |
NM_001114748.1:c.293T>A | NP_001108220.1:p.Phe98Tyr | |
NM_001114748.2:c.293T>A MANE Select | NP_001108220.1:p.Phe98Tyr |