HGVS | Genome Assembly |
---|---|
NC_000002.12:g.184915623A= , CM000664.2:g.184915623A= | GRCh38 |
NC_000002.11:g.185780350A= , CM000664.1:g.185780350A= | GRCh37 |
NC_000002.10:g.185488595A= | NCBI36 |
NG_046950.1:g.322258A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000302277.7:c.256-17980A= MANE Select | ENSP00000303252.6:n.256-17980A= | |
ENST00000302277.6:c.256-17980A= | ENSP00000303252.6:n.256-17980A= | |
ENST00000613975.1:c.1-17980A= | ENSP00000483032.1:n.1-17980A= | |
NM_194250.1:c.256-17980A= | NP_919226.1:n.256-17980A= | |
NM_194250.2:c.256-17980A= MANE Select | NP_919226.1:n.256-17980A= |