Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255929C= , CM000671.2:g.133255929C= | GRCh38 |
| NC_000009.11:g.136131316C= , CM000671.1:g.136131316C= | GRCh37 |
| NC_000009.10:g.135121137C= | NCBI36 |
| NG_006669.1:g.21739G= | |
| NG_006669.2:g.24287G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020469.2:c.802G= | NP_065202.2:p.Gly268= |
| NM_020469.3:c.802G= | NP_065202.2:p.Gly268= |
| ENST00000453660.3:n.813G= | |
| ENST00000453660.4:n.831G= | |
| ENST00000538324.2:c.799G= | ENSP00000483018.1:p.Gly267= |
| ENST00000611156.4:c.799G= | ENSP00000483265.1:p.Gly267= |
| ENST00000647353.1:n.54-4777G= | |
| ENST00000679909.1:c.28+19233G= | ENSP00000506089.1:n.28+19233G= |