HGVS | Genome Assembly |
---|---|
NC_000008.11:g.96145174G>T , CM000670.2:g.96145174G>T | GRCh38 |
NC_000008.10:g.97157402G>T , CM000670.1:g.97157402G>T | GRCh37 |
NC_000008.9:g.97226578G>T | NCBI36 |
NG_008981.1:g.20619C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000287020.7:c.757C>A MANE Select | ENSP00000287020.4:p.Gln253Lys | |
ENST00000287020.6:c.757C>A | ENSP00000287020.4:p.Gln253Lys | |
ENST00000620978.1:c.707-12C>A | ENSP00000480170.1:n.707-12C>A | |
ENST00000621429.1:c.757C>A | ENSP00000483711.1:p.Gln253Lys | |
NM_001001557.2:c.757C>A | NP_001001557.1:p.Gln253Lys | |
XM_011517030.1:c.358C>A | XP_011515332.1:p.Gln120Lys | |
NM_001001557.3:c.757C>A | NP_001001557.1:p.Gln253Lys | |
NM_001001557.4:c.757C>A MANE Select | NP_001001557.1:p.Gln253Lys |