Canonical Allele Identifier:
CA440675844
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542597T>C , CM000666.2:g.105542597T>C | GRCh38 |
| NC_000004.11:g.106463754T>C , CM000666.1:g.106463754T>C | GRCh37 |
| NC_000004.10:g.106683203T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.408A>G | ||
| XR_939039.1:n.568A>G | ||
| XR_939040.1:n.296-1121A>G | ||
| XR_001741410.1:n.423A>G | ||
| XR_001741411.1:n.899A>G | ||
| XR_001741412.1:n.423A>G | ||
| XR_001741413.1:n.423A>G | ||
| XR_001741414.1:n.423A>G | ||
| XR_939038.2:n.423A>G | ||
| XR_939040.2:n.311-1121A>G |