HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2444483G= , CM000673.2:g.2444483G= | GRCh38 |
NC_000011.9:g.2465713G= , CM000673.1:g.2465713G= | GRCh37 |
NC_000011.8:g.2422289G= | NCBI36 |
NG_008935.1:g.4493G= , LRG_287:g.4493G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696290.1:c.-1738C= MANE Select | ENSP00000512529.1:n.-1738C= | |
XR_930984.1:n.88C= | ||
NM_014555.4:c.-1738C= MANE Select | NP_055370.1:n.-1738C= |