Canonical Allele Identifier:
CA1948159609
Gene:
Linked Data
dbSNP Id:
rs1374998726
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2444543A>T , CM000673.2:g.2444543A>T | GRCh38 |
| NC_000011.9:g.2465773A>T , CM000673.1:g.2465773A>T | GRCh37 |
| NC_000011.8:g.2422349A>T | NCBI36 |
| NG_008935.1:g.4553A>T , LRG_287:g.4553A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930984.1:n.28T>A |