HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133256172G= , CM000671.2:g.133256172G= | GRCh38 |
NC_000009.11:g.136131559G= , CM000671.1:g.136131559G= | GRCh37 |
NC_000009.10:g.135121380G= | NCBI36 |
NG_006669.1:g.21496C= | |
NG_006669.2:g.24044C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.588C= | ||
ENST00000647353.1:n.54-5020C= | ||
ENST00000651471.1:n.514C= | ||
ENST00000679909.1:c.28+18990C= | ENSP00000506089.1:n.28+18990C= | |
ENST00000453660.3:n.570C= | ||
ENST00000538324.2:c.556C= | ENSP00000483018.1:p.Arg186= | |
ENST00000611156.4:c.556C= | ENSP00000483265.1:p.Arg186= | |
NM_020469.2:c.559C= | NP_065202.2:p.Arg187= | |
NM_020469.3:c.559C= | NP_065202.2:p.Arg187= |