HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52652033G= , CM000674.2:g.52652033G= | GRCh38 |
NC_000012.11:g.53045817G= , CM000674.1:g.53045817G= | GRCh37 |
NC_000012.10:g.51332084G= | NCBI36 |
NG_008296.1:g.5143C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309680.4:c.110C= MANE Select | ENSP00000310861.3:p.Thr37= | |
ENST00000309680.3:c.110C= | ENSP00000310861.3:p.Thr37= | |
NM_000423.2:c.110C= | NP_000414.2:p.Thr37= | |
NM_000423.3:c.110C= MANE Select | NP_000414.2:p.Thr37= |