Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8733453C>A , CM000665.2:g.8733453C>A | GRCh38 |
| NC_000003.11:g.8775139C>A , CM000665.1:g.8775139C>A | GRCh37 |
| NC_000003.10:g.8750139C>A | NCBI36 |
| NG_008797.2:g.4644C>A , LRG_329:g.4644C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435138.5:c.64+9006G>T | ENSP00000412333.1:n.64+9006G>T | |
| ENST00000478513.1:n.335+9006G>T | ||
| XR_940435.1:n.330+9006G>T | ||
| XM_017006530.1:c.-283+9006G>T | XP_016862019.1:n.-283+9006G>T |