HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31810495G>A , CM000668.2:g.31810495G>A | GRCh38 |
NC_000006.11:g.31778272G>A , CM000668.1:g.31778272G>A | GRCh37 |
NC_000006.10:g.31886251G>A | NCBI36 |
NG_011855.1:g.9564C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375654.5:c.1478C>T MANE Select | ENSP00000364805.4:p.Thr493Met | |
ENST00000375654.4:c.1478C>T | ENSP00000364805.4:p.Thr493Met | |
NM_005527.3:c.1478C>T | NP_005518.3:p.Thr493Met | |
XM_005249070.3:c.1670C>T | XP_005249127.1:p.Thr557Met | |
XM_005249071.1:c.1478C>T | XP_005249128.1:p.Thr493Met | |
XM_005249073.2:c.1478C>T | XP_005249130.1:p.Thr493Met | |
XM_011514566.1:c.1478C>T | XP_011512868.1:p.Thr493Met | |
NM_005527.4:c.1478C>T MANE Select | NP_005518.3:p.Thr493Met |