Canonical Allele Identifier: CA1715429652
Gene:

Linked Data

dbSNP Id: rs1788208400

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146935C>G , CM000669.2:g.69146935C>G GRCh38
NC_000007.13:g.68611922C>G , CM000669.1:g.68611922C>G GRCh37
NC_000007.12:g.68249858C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-809G>C