HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52652159G= , CM000674.2:g.52652159G= | GRCh38 |
NC_000012.11:g.53045943G= , CM000674.1:g.53045943G= | GRCh37 |
NC_000012.10:g.51332210G= | NCBI36 |
NG_008296.1:g.5017C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309680.4:c.-17C= MANE Select | ENSP00000310861.3:n.-17C= | |
ENST00000309680.3:c.-17C= | ENSP00000310861.3:n.-17C= | |
NM_000423.2:c.-17C= | NP_000414.2:n.-17C= | |
NM_000423.3:c.-17C= MANE Select | NP_000414.2:n.-17C= |