Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.78317873T>G , CM000671.2:g.78317873T>G | GRCh38 |
| NC_000009.11:g.80932789T>G , CM000671.1:g.80932789T>G | GRCh37 |
| NC_000009.10:g.80122609T>G | NCBI36 |
| NG_012165.1:g.25731T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_058179.4:c.869+69T>G MANE Select | NP_478059.1:n.869+69T>G |
| ENST00000376588.4:c.869+69T>G MANE Select | ENSP00000365773.3:n.869+69T>G |
| NM_021154.4:c.869+69T>G | NP_066977.1:n.869+69T>G |
| NM_021154.5:c.869+69T>G | NP_066977.1:n.869+69T>G |
| NM_058179.3:c.869+69T>G | NP_478059.1:n.869+69T>G |
| ENST00000347159.6:c.869+69T>G | ENSP00000317606.2:n.869+69T>G |
| ENST00000376588.3:c.869+69T>G | ENSP00000365773.3:n.869+69T>G |