Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129819001G>A , CM000671.2:g.129819001G>A | GRCh38 |
| NC_000009.11:g.132581280G>A , CM000671.1:g.132581280G>A | GRCh37 |
| NC_000009.10:g.131621101G>A | NCBI36 |
| NG_008049.1:g.10162C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.445-81C>T MANE Select | ENSP00000345719.4:n.445-81C>T | |
| ENST00000651202.1:c.541-81C>T | ENSP00000498222.1:n.541-81C>T | |
| ENST00000351698.4:c.445-81C>T | ENSP00000345719.4:n.445-81C>T | |
| ENST00000473604.2:n.555-81C>T | ||
| NM_000113.2:c.445-81C>T | NP_000104.1:n.445-81C>T | |
| XR_929731.1:n.605-81C>T | ||
| XR_929731.3:n.473-81C>T | ||
| NM_000113.3:c.445-81C>T MANE Select | NP_000104.1:n.445-81C>T |