Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.93998166A>C , CM000663.2:g.93998166A>C | GRCh38 |
| NC_000001.10:g.94463722A>C , CM000663.1:g.94463722A>C | GRCh37 |
| NC_000001.9:g.94236310A>C | NCBI36 |
| NG_009073.1:g.127984T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6480-56T>G MANE Select | ENSP00000359245.3:n.6480-56T>G | |
| ENST00000370225.3:c.6480-56T>G | ENSP00000359245.3:n.6480-56T>G | |
| ENST00000536513.5:c.2856-56T>G | ENSP00000439707.2:n.2856-56T>G | |
| NM_000350.2:c.6480-56T>G | NP_000341.2:n.6480-56T>G | |
| NM_000350.3:c.6480-56T>G MANE Select | NP_000341.2:n.6480-56T>G |