Canonical Allele Identifier: CA1462694070
Gene:

Linked Data

dbSNP Id: rs1756224058
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557831C>A , CM000666.2:g.62557831C>A GRCh38
NC_000004.11:g.63423549C>A , CM000666.1:g.63423549C>A GRCh37
NC_000004.10:g.63106144C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-6013C>A
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