Canonical Allele Identifier: CA1715429797
Gene:

Linked Data

dbSNP Id: rs1427647816

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146985T>A , CM000669.2:g.69146985T>A GRCh38
NC_000007.13:g.68611972T>A , CM000669.1:g.68611972T>A GRCh37
NC_000007.12:g.68249908T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-859A>T