HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114713941G= , CM000663.2:g.114713941G= | GRCh38 |
NC_000001.10:g.115256562G= , CM000663.1:g.115256562G= | GRCh37 |
NC_000001.9:g.115058085G= | NCBI36 |
NG_007572.1:g.7954C= , LRG_92:g.7954C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.149C= MANE Select | ENSP00000358548.4:p.Thr50= | |
ENST00000369535.4:c.149C= | ENSP00000358548.4:p.Thr50= | |
NM_002524.4:c.149C= | NP_002515.1:p.Thr50= | |
NM_002524.5:c.149C= MANE Select | NP_002515.1:p.Thr50= |