HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2444481G= , CM000673.2:g.2444481G= | GRCh38 |
NC_000011.9:g.2465711G= , CM000673.1:g.2465711G= | GRCh37 |
NC_000011.8:g.2422287G= | NCBI36 |
NG_008935.1:g.4491G= , LRG_287:g.4491G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696290.1:c.-1736C= MANE Select | ENSP00000512529.1:n.-1736C= | |
XR_930984.1:n.90C= | ||
NM_014555.4:c.-1736C= MANE Select | NP_055370.1:n.-1736C= |