HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48474614C>A , CM000677.2:g.48474614C>A | GRCh38 |
NC_000015.9:g.48766811C>A , CM000677.1:g.48766811C>A | GRCh37 |
NC_000015.8:g.46554103C>A | NCBI36 |
NG_008805.2:g.176175G>T , LRG_778:g.176175G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.4001G>T | ENSP00000453958.2:p.Gly1334Val | |
ENST00000674301.2:c.4001G>T | ENSP00000501333.2:p.Gly1334Val | |
ENST00000684448.1:n.2675G>T | ||
ENST00000316623.10:c.4001G>T MANE Select | ENSP00000325527.5:p.Gly1334Val | |
ENST00000316623.9:c.4001G>T | ENSP00000325527.5:p.Gly1334Val | |
ENST00000537463.6:c.673G>T | ENSP00000440294.2:p.Ala225Ser | |
NM_000138.4:c.4001G>T , LRG_778t1:c.4001G>T | NP_000129.3:p.Gly1334Val | |
NM_000138.5:c.4001G>T MANE Select | NP_000129.3:p.Gly1334Val |