Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133256323C= , CM000671.2:g.133256323C= | GRCh38 |
| NC_000009.11:g.136131710C= , CM000671.1:g.136131710C= | GRCh37 |
| NC_000009.10:g.135121531C= | NCBI36 |
| NG_006669.1:g.21345G= | |
| NG_006669.2:g.23893G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.437G= | ||
| ENST00000647353.1:n.54-5171G= | ||
| ENST00000651471.1:n.363G= | ||
| ENST00000679909.1:c.28+18839G= | ENSP00000506089.1:n.28+18839G= | |
| ENST00000453660.3:n.419G= | ||
| ENST00000538324.2:c.405G= | ENSP00000483018.1:p.Thr135= | |
| ENST00000611156.4:c.405G= | ENSP00000483265.1:p.Thr135= | |
| NM_020469.2:c.408G= | NP_065202.2:p.Thr136= | |
| NM_020469.3:c.408G= | NP_065202.2:p.Thr136= |