HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189058889A>T , CM000664.2:g.189058889A>T | GRCh38 |
NC_000002.11:g.189923615A>T , CM000664.1:g.189923615A>T | GRCh37 |
NC_000002.10:g.189631860A>T | NCBI36 |
NG_011799.1:g.125991T>A | |
NG_011799.2:g.125991T>A | |
NG_011799.3:g.171413T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000374866.9:c.2090T>A MANE Select | ENSP00000364000.3:p.Val697Asp | |
ENST00000374866.7:c.2090T>A | ENSP00000364000.3:p.Val697Asp | |
ENST00000470524.2:n.196T>A | ||
ENST00000618828.1:c.929T>A | ENSP00000482184.1:p.Val310Asp | |
NM_000393.3:c.2090T>A | NP_000384.2:p.Val697Asp | |
XM_011510573.1:c.1952T>A | XP_011508875.1:p.Val651Asp | |
NM_000393.4:c.2090T>A | NP_000384.2:p.Val697Asp | |
XM_011510573.3:c.1952T>A | XP_011508875.1:p.Val651Asp | |
NM_000393.5:c.2090T>A MANE Select | NP_000384.2:p.Val697Asp |