Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98542033G>T , CM000671.2:g.98542033G>T | GRCh38 |
| NC_000009.11:g.101304315G>T , CM000671.1:g.101304315G>T | GRCh37 |
| NC_000009.10:g.100344136G>T | NCBI36 |
| NG_016426.1:g.172165C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.470C>A MANE Select | ENSP00000259455.2:p.Ala157Asp | |
| ENST00000637410.1:n.248C>A | ||
| ENST00000637717.1:c.86C>A | ENSP00000490789.1:p.Ala29Asp | |
| ENST00000638001.1:n.80C>A | ||
| ENST00000259455.3:c.470C>A | ENSP00000259455.2:p.Ala157Asp | |
| ENST00000477471.1:n.257C>A | ||
| ENST00000634227.1:n.244C>A | ||
| NM_005458.7:c.470C>A | NP_005449.5:p.Ala157Asp | |
| XM_017015331.2:c.176C>A | XP_016870820.1:p.Ala59Asp | |
| NM_005458.8:c.470C>A MANE Select | NP_005449.5:p.Ala157Asp |