Canonical Allele Identifier: CA797158459
Gene:

Linked Data

dbSNP Id: rs1215004954
MyVariant Identifiers: chr4:g.63423605C>A (hg19) chr4:g.62557887C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557887C>A , CM000666.2:g.62557887C>A GRCh38
NC_000004.11:g.63423605C>A , CM000666.1:g.63423605C>A GRCh37
NC_000004.10:g.63106200C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5957C>A
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