Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149926325T>C , CM000663.2:g.149926325T>C | GRCh38 |
| NC_000001.10:g.149898217T>C , CM000663.1:g.149898217T>C | GRCh37 |
| NC_000001.9:g.148164841T>C | NCBI36 |
| NG_032777.1:g.6928A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.9:c.706+51A>G MANE Select | ENSP00000271628.8:n.706+51A>G | |
| ENST00000271628.8:c.706+51A>G | ENSP00000271628.8:n.706+51A>G | |
| NM_005850.4:c.706+51A>G | NP_005841.1:n.706+51A>G | |
| NM_005850.5:c.706+51A>G MANE Select | NP_005841.1:n.706+51A>G |