Canonical Allele Identifier: CA98367522
Gene:

Linked Data

dbSNP Id: rs1032847116
MyVariant Identifiers: chr4:g.63423653C>A (hg19) chr4:g.62557935C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557935C>A , CM000666.2:g.62557935C>A GRCh38
NC_000004.11:g.63423653C>A , CM000666.1:g.63423653C>A GRCh37
NC_000004.10:g.63106248C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5909C>A
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