HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88008064G= , CM000666.2:g.88008064G= | GRCh38 |
NC_000004.11:g.88929216G= , CM000666.1:g.88929216G= | GRCh37 |
NC_000004.10:g.89148240G= | NCBI36 |
NG_008604.1:g.5397G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.331G= MANE Select | ENSP00000237596.2:p.Val111= | |
ENST00000237596.6:c.331G= | ENSP00000237596.2:p.Val111= | |
NM_000297.3:c.331G= | NP_000288.1:p.Val111= | |
XM_011532028.1:c.331G= | XP_011530330.1:p.Val111= | |
XR_244632.2:n.426G= | ||
NR_156488.1:n.418G= | ||
XM_011532028.2:c.331G= | XP_011530330.1:p.Val111= | |
NM_000297.4:c.331G= MANE Select | NP_000288.1:p.Val111= | |
NR_156488.2:n.430G= |