HGVS | Genome Assembly |
---|---|
NC_000002.12:g.223053491G= , CM000664.2:g.223053491G= | GRCh38 |
NC_000002.11:g.223918209G= , CM000664.1:g.223918209G= | GRCh37 |
NC_000002.10:g.223626453G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000281830.4:c.*148G= MANE Select | ENSP00000281830.5:n.*148G= | |
ENST00000281830.3:c.*148G= | ENSP00000281830.4:n.*148G= | |
ENST00000488477.2:n.75+1217G= | ||
NM_080671.3:c.*148G= | NP_542402.3:n.*148G= | |
NM_080671.4:c.*148G= MANE Select | NP_542402.4:n.*148G= |