Canonical Allele Identifier:
CA1482797502
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542519T= , CM000666.2:g.105542519T= | GRCh38 |
| NC_000004.11:g.106463676T= , CM000666.1:g.106463676T= | GRCh37 |
| NC_000004.10:g.106683125T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.486A= | ||
| XR_939039.1:n.646A= | ||
| XR_939040.1:n.296-1043A= | ||
| XR_001741410.1:n.501A= | ||
| XR_001741411.1:n.977A= | ||
| XR_001741412.1:n.449+52A= | ||
| XR_001741413.1:n.501A= | ||
| XR_001741414.1:n.449+52A= | ||
| XR_939038.2:n.501A= | ||
| XR_939040.2:n.311-1043A= |