HGVS | Genome Assembly |
---|---|
NC_000002.12:g.70831736C= , CM000664.2:g.70831736C= | GRCh38 |
NC_000002.11:g.71058867C= , CM000664.1:g.71058867C= | GRCh37 |
NC_000002.10:g.70912375C= | NCBI36 |
NG_033914.1:g.9088G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000410009.5:c.801G= MANE Select | ENSP00000386378.3:p.Val267= | |
ENST00000410009.4:c.801G= | ENSP00000386378.3:p.Val267= | |
NM_015717.4:c.801G= | NP_056532.4:p.Val267= | |
XM_011532874.1:c.801G= | XP_011531176.1:p.Val267= | |
XM_011532875.1:c.801G= | XP_011531177.1:p.Val267= | |
XM_011532876.1:c.801G= | XP_011531178.1:p.Val267= | |
XM_011532875.2:c.801G= | XP_011531177.1:p.Val267= | |
XM_011532876.2:c.801G= | XP_011531178.1:p.Val267= | |
NM_015717.5:c.801G= MANE Select | NP_056532.4:p.Val267= |