Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133256218T= , CM000671.2:g.133256218T= | GRCh38 |
| NC_000009.11:g.136131605T= , CM000671.1:g.136131605T= | GRCh37 |
| NC_000009.10:g.135121426T= | NCBI36 |
| NG_006669.1:g.21450A= | |
| NG_006669.2:g.23998A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.542A= | ||
| ENST00000647353.1:n.54-5066A= | ||
| ENST00000651471.1:n.468A= | ||
| ENST00000679909.1:c.28+18944A= | ENSP00000506089.1:n.28+18944A= | |
| ENST00000453660.3:n.524A= | ||
| ENST00000538324.2:c.510A= | ENSP00000483018.1:p.Ser170= | |
| ENST00000611156.4:c.510A= | ENSP00000483265.1:p.Ser170= | |
| NM_020469.2:c.513A= | NP_065202.2:p.Ser171= | |
| NM_020469.3:c.513A= | NP_065202.2:p.Ser171= |