Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255839C= , CM000671.2:g.133255839C= | GRCh38 |
| NC_000009.11:g.136131226C= , CM000671.1:g.136131226C= | GRCh37 |
| NC_000009.10:g.135121047C= | NCBI36 |
| NG_006669.1:g.21829G= | |
| NG_006669.2:g.24377G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.921G= | ||
| ENST00000647353.1:n.54-4687G= | ||
| ENST00000679909.1:c.28+19323G= | ENSP00000506089.1:n.28+19323G= | |
| ENST00000453660.3:n.903G= | ||
| ENST00000538324.2:c.889G= | ENSP00000483018.1:p.Ala297= | |
| ENST00000611156.4:c.889G= | ENSP00000483265.1:p.Ala297= | |
| NM_020469.2:c.892G= | NP_065202.2:p.Ala298= | |
| NM_020469.3:c.892G= | NP_065202.2:p.Ala298= |