HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65958011G= , CM000674.2:g.65958011G= | GRCh38 |
NC_000012.11:g.66351791G= , CM000674.1:g.66351791G= | GRCh37 |
NC_000012.10:g.64638058G= | NCBI36 |
NG_016296.1:g.138552G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000403681.7:c.283-5234G= MANE Select | ENSP00000384026.2:n.283-5234G= | |
ENST00000403681.6:c.283-5234G= | ENSP00000384026.2:n.283-5234G= | |
ENST00000539662.1:c.320-5234G= | ENSP00000440919.1:n.320-5234G= | |
ENST00000541363.5:c.*6578G= | ENSP00000439317.1:n.*6578G= | |
NM_003483.4:c.283-5234G= | NP_003474.1:n.283-5234G= | |
NM_003483.6:c.283-5234G= MANE Select | NP_003474.1:n.283-5234G= |