Canonical Allele Identifier: CA1462694089
Gene:

Linked Data

dbSNP Id: rs1577990855
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557866T>A , CM000666.2:g.62557866T>A GRCh38
NC_000004.11:g.63423584T>A , CM000666.1:g.63423584T>A GRCh37
NC_000004.10:g.63106179T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5978T>A
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Search 100 bp 3'