Canonical Allele Identifier: CA1259578664
Gene:

Linked Data

dbSNP Id: rs1669749047

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70438448C>A , CM000664.2:g.70438448C>A GRCh38
NC_000002.11:g.70665580C>A , CM000664.1:g.70665580C>A GRCh37
NC_000002.10:g.70519088C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940229.1:n.230-2852C>A