HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135320A= , CM000664.2:g.26135320A= | GRCh38 |
NC_000002.11:g.26358189A= , CM000664.1:g.26358189A= | GRCh37 |
NC_000002.10:g.26211693A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264710.5:c.*299A= MANE Select | ENSP00000264710.4:n.*299A= | |
ENST00000264710.4:c.*299A= | ENSP00000264710.4:n.*299A= | |
ENST00000495146.5:n.1265A= | ||
NM_016131.4:c.*299A= | NP_057215.3:n.*299A= | |
XM_024452565.1:c.*299A= | XP_024308333.1:n.*299A= | |
NM_016131.5:c.*299A= MANE Select | NP_057215.3:n.*299A= |