Canonical Allele Identifier: CA1963413383
Gene:

Linked Data

dbSNP Id: rs1851776791

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812624A>C , CM000673.2:g.34812624A>C GRCh38
NC_000011.9:g.34834171A>C , CM000673.1:g.34834171A>C GRCh37
NC_000011.8:g.34790747A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+58017A>C
XR_931188.1:n.693+58017A>C
XR_931189.1:n.854+58017A>C
XR_931190.1:n.639+58017A>C
XR_931191.1:n.689+58017A>C
XR_001748174.1:n.855+58017A>C
XR_001748176.1:n.1016+58017A>C
XR_002957246.1:n.639+58017A>C