HGVS | Genome Assembly |
---|---|
NC_000007.14:g.95318530T= , CM000669.2:g.95318530T= | GRCh38 |
NC_000007.13:g.94947842T= , CM000669.1:g.94947842T= | GRCh37 |
NC_000007.12:g.94785778T= | NCBI36 |
NG_008779.1:g.11043A= | |
NG_008779.2:g.11177A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222381.8:c.75-137A= MANE Select | ENSP00000222381.3:n.75-137A= | |
ENST00000222381.7:c.75-137A= | ENSP00000222381.3:n.75-137A= | |
ENST00000433729.1:c.75-137A= | ENSP00000407359.1:n.75-137A= | |
ENST00000470502.1:n.58A= | ||
NM_000446.5:c.75-137A= | NP_000437.3:n.75-137A= | |
NM_000446.6:c.75-137A= | NP_000437.3:n.75-137A= | |
NM_000446.7:c.75-137A= MANE Select | NP_000437.3:n.75-137A= |