Canonical Allele Identifier:
CA1205765949
Gene:
Linked Data
dbSNP Id:
rs1648342522
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.168649252C>T , CM000663.2:g.168649252C>T | GRCh38 |
| NC_000001.10:g.168618490C>T , CM000663.1:g.168618490C>T | GRCh37 |
| NC_000001.9:g.166885114C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922259.1:n.201-7977G>A | ||
| XR_922259.2:n.332-7977G>A |