Canonical Allele Identifier: CA2563257537
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812268G>C , CM000673.2:g.34812268G>C GRCh38
NC_000011.9:g.34833815G>C , CM000673.1:g.34833815G>C GRCh37
NC_000011.8:g.34790391G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+57661G>C
XR_931188.1:n.693+57661G>C
XR_931189.1:n.854+57661G>C
XR_931190.1:n.639+57661G>C
XR_931191.1:n.689+57661G>C
XR_001748174.1:n.855+57661G>C
XR_001748176.1:n.1016+57661G>C
XR_002957246.1:n.639+57661G>C