Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29920005T>C , CM000664.2:g.29920005T>C | GRCh38 |
| NC_000002.11:g.30142871T>C , CM000664.1:g.30142871T>C | GRCh37 |
| NC_000002.10:g.29996375T>C | NCBI36 |
| NG_009445.1:g.6562A>G , LRG_488:g.6562A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004304.5:c.655A>G MANE Select | NP_004295.2:p.Ile219Val |
| ENST00000389048.8:c.655A>G MANE Select | ENSP00000373700.3:p.Ile219Val |
| NM_004304.4:c.655A>G | NP_004295.2:p.Ile219Val |
| ENST00000389048.7:c.655A>G | ENSP00000373700.3:p.Ile219Val |
| XR_001738688.2:n.1585A>G |