Canonical Allele Identifier: CA1732296747
Gene:

Linked Data

dbSNP Id: rs342293

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.106731773C>A , CM000669.2:g.106731773C>A GRCh38
NC_000007.13:g.106372219C>A , CM000669.1:g.106372219C>A GRCh37
NC_000007.12:g.106159455C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745317.1:n.119+569G>T