Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94030933A>C , CM000663.2:g.94030933A>C | GRCh38 |
| NC_000001.10:g.94496489A>C , CM000663.1:g.94496489A>C | GRCh37 |
| NC_000001.9:g.94269077A>C | NCBI36 |
| NG_009073.1:g.95217T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370225.4:c.4253+63T>G MANE Select | ENSP00000359245.3:n.4253+63T>G | |
| ENST00000370225.3:c.4253+63T>G | ENSP00000359245.3:n.4253+63T>G | |
| ENST00000536513.5:c.629+63T>G | ENSP00000439707.2:n.629+63T>G | |
| NM_000350.2:c.4253+63T>G | NP_000341.2:n.4253+63T>G | |
| NM_000350.3:c.4253+63T>G MANE Select | NP_000341.2:n.4253+63T>G |