Canonical Allele Identifier: CA1963413385
Gene:

Linked Data

dbSNP Id: rs1851776818

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812629T>A , CM000673.2:g.34812629T>A GRCh38
NC_000011.9:g.34834176T>A , CM000673.1:g.34834176T>A GRCh37
NC_000011.8:g.34790752T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+58022T>A
XR_931188.1:n.693+58022T>A
XR_931189.1:n.854+58022T>A
XR_931190.1:n.639+58022T>A
XR_931191.1:n.689+58022T>A
XR_001748174.1:n.855+58022T>A
XR_001748176.1:n.1016+58022T>A
XR_002957246.1:n.639+58022T>A