HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154928752C= , CM000685.2:g.154928752C= | GRCh38 |
NC_000023.10:g.154157027C= , CM000685.1:g.154157027C= | GRCh37 |
NC_000023.9:g.153810221C= | NCBI36 |
NG_011403.1:g.98972G= | |
NG_011403.2:g.98972G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.5038G= MANE Select | ENSP00000353393.4:p.Glu1680= | |
ENST00000360256.8:c.5038G= | ENSP00000353393.4:p.Glu1680= | |
NM_000132.3:c.5038G= | NP_000123.1:p.Glu1680= | |
XM_011531126.1:c.4933G= | XP_011529428.1:p.Glu1645= | |
NM_000132.4:c.5038G= MANE Select | NP_000123.1:p.Glu1680= |