HGVS | Genome Assembly |
---|---|
NC_000010.11:g.68231635C>A , CM000672.2:g.68231635C>A | GRCh38 |
NC_000010.10:g.69991392C>A , CM000672.1:g.69991392C>A | GRCh37 |
NC_000010.9:g.69661398C>A | NCBI36 |
NG_031934.1:g.5479G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373673.5:c.43G>T MANE Select | ENSP00000362777.3:p.Val15Phe | |
ENST00000373673.4:c.43G>T | ENSP00000362777.3:p.Val15Phe | |
NM_145178.3:c.43G>T | NP_660161.1:p.Val15Phe | |
NM_145178.4:c.43G>T MANE Select | NP_660161.1:p.Val15Phe |