HGVS | Genome Assembly |
---|---|
NC_000004.12:g.119320788A>T , CM000666.2:g.119320788A>T | GRCh38 |
NC_000004.11:g.120241943A>T , CM000666.1:g.120241943A>T | GRCh37 |
NC_000004.10:g.120461391A>T | NCBI36 |
NG_011444.1:g.6374T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274024.4:c.122T>A MANE Select | ENSP00000274024.3:p.Ile41Asn | |
ENST00000274024.3:c.122T>A | ENSP00000274024.3:p.Ile41Asn | |
NM_000134.3:c.122T>A | NP_000125.2:p.Ile41Asn | |
NM_000134.4:c.122T>A MANE Select | NP_000125.2:p.Ile41Asn |