Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133256267T= , CM000671.2:g.133256267T= | GRCh38 |
| NC_000009.11:g.136131654T= , CM000671.1:g.136131654T= | GRCh37 |
| NC_000009.10:g.135121475T= | NCBI36 |
| NG_006669.1:g.21401A= | |
| NG_006669.2:g.23949A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.493A= | ||
| ENST00000647353.1:n.54-5115A= | ||
| ENST00000651471.1:n.419A= | ||
| ENST00000679909.1:c.28+18895A= | ENSP00000506089.1:n.28+18895A= | |
| ENST00000453660.3:n.475A= | ||
| ENST00000538324.2:c.461A= | ENSP00000483018.1:p.Gln154= | |
| ENST00000611156.4:c.461A= | ENSP00000483265.1:p.Gln154= | |
| NM_020469.2:c.464A= | NP_065202.2:p.Gln155= | |
| NM_020469.3:c.464A= | NP_065202.2:p.Gln155= |