HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70175794T>A , CM000679.2:g.70175794T>A | GRCh38 |
NC_000017.10:g.68171935T>A , CM000679.1:g.68171935T>A | GRCh37 |
NC_000017.9:g.65683530T>A | NCBI36 |
NG_008798.1:g.11260T>A , LRG_328:g.11260T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243457.4:c.755T>A MANE Select | ENSP00000243457.2:p.Val252Asp | |
ENST00000243457.3:c.755T>A | ENSP00000243457.2:p.Val252Asp | |
ENST00000535240.1:c.755T>A | ENSP00000441848.1:p.Val252Asp | |
NM_000891.2:c.755T>A , LRG_328t1:c.755T>A | NP_000882.1:p.Val252Asp | |
XM_011524779.1:c.755T>A | XP_011523081.1:p.Val252Asp | |
NM_000891.3:c.755T>A MANE Select | NP_000882.1:p.Val252Asp |