Canonical Allele Identifier:
CA103381282
Gene:
Linked Data
dbSNP Id:
rs992012866
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.105542504T>C , CM000666.2:g.105542504T>C | GRCh38 |
| NC_000004.11:g.106463661T>C , CM000666.1:g.106463661T>C | GRCh37 |
| NC_000004.10:g.106683110T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939038.1:n.501A>G | ||
| XR_939039.1:n.661A>G | ||
| XR_939040.1:n.296-1028A>G | ||
| XR_001741410.1:n.516A>G | ||
| XR_001741411.1:n.992A>G | ||
| XR_001741412.1:n.449+67A>G | ||
| XR_001741413.1:n.516A>G | ||
| XR_001741414.1:n.449+67A>G | ||
| XR_939038.2:n.516A>G | ||
| XR_939040.2:n.311-1028A>G |