HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135339T= , CM000664.2:g.26135339T= | GRCh38 |
NC_000002.11:g.26358208T= , CM000664.1:g.26358208T= | GRCh37 |
NC_000002.10:g.26211712T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264710.5:c.*318T= MANE Select | ENSP00000264710.4:n.*318T= | |
ENST00000264710.4:c.*318T= | ENSP00000264710.4:n.*318T= | |
ENST00000495146.5:n.1284T= | ||
NM_016131.4:c.*318T= | NP_057215.3:n.*318T= | |
XM_024452565.1:c.*318T= | XP_024308333.1:n.*318T= | |
NM_016131.5:c.*318T= MANE Select | NP_057215.3:n.*318T= |