Canonical Allele Identifier: CA1963413398
Gene:

Linked Data

dbSNP Id: rs1851777121

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812658G>A , CM000673.2:g.34812658G>A GRCh38
NC_000011.9:g.34834205G>A , CM000673.1:g.34834205G>A GRCh37
NC_000011.8:g.34790781G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+58051G>A
XR_931188.1:n.693+58051G>A
XR_931189.1:n.854+58051G>A
XR_931190.1:n.639+58051G>A
XR_931191.1:n.689+58051G>A
XR_001748174.1:n.855+58051G>A
XR_001748176.1:n.1016+58051G>A
XR_002957246.1:n.639+58051G>A