Canonical Allele Identifier:
CA2762952391
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542538T>C , CM000666.2:g.105542538T>C | GRCh38 |
| NC_000004.11:g.106463695T>C , CM000666.1:g.106463695T>C | GRCh37 |
| NC_000004.10:g.106683144T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.467A>G | ||
| XR_939039.1:n.627A>G | ||
| XR_939040.1:n.296-1062A>G | ||
| XR_001741410.1:n.482A>G | ||
| XR_001741411.1:n.958A>G | ||
| XR_001741412.1:n.449+33A>G | ||
| XR_001741413.1:n.482A>G | ||
| XR_001741414.1:n.449+33A>G | ||
| XR_939038.2:n.482A>G | ||
| XR_939040.2:n.311-1062A>G |