HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31810495G>C , CM000668.2:g.31810495G>C | GRCh38 |
NC_000006.11:g.31778272G>C , CM000668.1:g.31778272G>C | GRCh37 |
NC_000006.10:g.31886251G>C | NCBI36 |
NG_011855.1:g.9564C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375654.5:c.1478C>G MANE Select | ENSP00000364805.4:p.Thr493Arg | |
ENST00000375654.4:c.1478C>G | ENSP00000364805.4:p.Thr493Arg | |
NM_005527.3:c.1478C>G | NP_005518.3:p.Thr493Arg | |
XM_005249070.3:c.1670C>G | XP_005249127.1:p.Thr557Arg | |
XM_005249071.1:c.1478C>G | XP_005249128.1:p.Thr493Arg | |
XM_005249073.2:c.1478C>G | XP_005249130.1:p.Thr493Arg | |
XM_011514566.1:c.1478C>G | XP_011512868.1:p.Thr493Arg | |
NM_005527.4:c.1478C>G MANE Select | NP_005518.3:p.Thr493Arg |