Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94078678T>C , CM000663.2:g.94078678T>C | GRCh38 |
| NC_000001.10:g.94544234T>C , CM000663.1:g.94544234T>C | GRCh37 |
| NC_000001.9:g.94316822T>C | NCBI36 |
| NG_009073.1:g.47472A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.1268A>G MANE Select | ENSP00000359245.3:p.His423Arg | |
| ENST00000649773.1:c.1268A>G | ENSP00000496882.1:p.His423Arg | |
| ENST00000370225.3:c.1268A>G | ENSP00000359245.3:p.His423Arg | |
| NM_000350.2:c.1268A>G | NP_000341.2:p.His423Arg | |
| NM_000350.3:c.1268A>G MANE Select | NP_000341.2:p.His423Arg |