Canonical Allele Identifier: CA1963376097
Gene:

Linked Data

dbSNP Id: rs1851019468
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759499C>A , CM000673.2:g.34759499C>A GRCh38
NC_000011.9:g.34781046C>A , CM000673.1:g.34781046C>A GRCh37
NC_000011.8:g.34737622C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+4892C>A
XR_931188.1:n.693+4892C>A
XR_931189.1:n.854+4892C>A
XR_931190.1:n.639+4892C>A
XR_931191.1:n.689+4892C>A
XR_001748174.1:n.855+4892C>A
XR_001748176.1:n.1016+4892C>A
XR_002957246.1:n.639+4892C>A
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