Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255921G= , CM000671.2:g.133255921G= | GRCh38 |
| NC_000009.11:g.136131308G= , CM000671.1:g.136131308G= | GRCh37 |
| NC_000009.10:g.135121129G= | NCBI36 |
| NG_006669.1:g.21747C= | |
| NG_006669.2:g.24295C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.839C= | ||
| ENST00000647353.1:n.54-4769C= | ||
| ENST00000679909.1:c.28+19241C= | ENSP00000506089.1:n.28+19241C= | |
| ENST00000453660.3:n.821C= | ||
| ENST00000538324.2:c.807C= | ENSP00000483018.1:p.Phe269= | |
| ENST00000611156.4:c.807C= | ENSP00000483265.1:p.Phe269= | |
| NM_020469.2:c.810C= | NP_065202.2:p.Phe270= | |
| NM_020469.3:c.810C= | NP_065202.2:p.Phe270= |