HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135317C= , CM000664.2:g.26135317C= | GRCh38 |
NC_000002.11:g.26358186C= , CM000664.1:g.26358186C= | GRCh37 |
NC_000002.10:g.26211690C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264710.5:c.*296C= MANE Select | ENSP00000264710.4:n.*296C= | |
ENST00000264710.4:c.*296C= | ENSP00000264710.4:n.*296C= | |
ENST00000495146.5:n.1262C= | ||
NM_016131.4:c.*296C= | NP_057215.3:n.*296C= | |
XM_024452565.1:c.*296C= | XP_024308333.1:n.*296C= | |
NM_016131.5:c.*296C= MANE Select | NP_057215.3:n.*296C= |