Canonical Allele Identifier: CA1715429616
Gene:

Linked Data

dbSNP Id: rs1788208128

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146908G>A , CM000669.2:g.69146908G>A GRCh38
NC_000007.13:g.68611895G>A , CM000669.1:g.68611895G>A GRCh37
NC_000007.12:g.68249831G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-782C>T