Canonical Allele Identifier:
CA2072411505
Gene:
Linked Data
dbSNP Id:
rs1953652383
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.131529616A>T , CM000674.2:g.131529616A>T | GRCh38 |
| NC_000012.11:g.132014161A>T , CM000674.1:g.132014161A>T | GRCh37 |
| NC_000012.10:g.130580114A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_945564.1:n.1076+159T>A | ||
| XR_001749407.2:n.1067+159T>A |