Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149926225T>G , CM000663.2:g.149926225T>G | GRCh38 |
| NC_000001.10:g.149898117T>G , CM000663.1:g.149898117T>G | GRCh37 |
| NC_000001.9:g.148164741T>G | NCBI36 |
| NG_032777.1:g.7028A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.9:c.706+151A>C MANE Select | ENSP00000271628.8:n.706+151A>C | |
| ENST00000271628.8:c.706+151A>C | ENSP00000271628.8:n.706+151A>C | |
| NM_005850.4:c.706+151A>C | NP_005841.1:n.706+151A>C | |
| NM_005850.5:c.706+151A>C MANE Select | NP_005841.1:n.706+151A>C |