Canonical Allele Identifier: CA797158726
Gene:

Linked Data

dbSNP Id: rs1454791540
MyVariant Identifiers: chr4:g.63424025G>A (hg19) chr4:g.62558307G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558307G>A , CM000666.2:g.62558307G>A GRCh38
NC_000004.11:g.63424025G>A , CM000666.1:g.63424025G>A GRCh37
NC_000004.10:g.63106620G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5537G>A
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