Canonical Allele Identifier: CA1462694074
Gene:

Linked Data

dbSNP Id: rs1756224123
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557835C>T , CM000666.2:g.62557835C>T GRCh38
NC_000004.11:g.63423553C>T , CM000666.1:g.63423553C>T GRCh37
NC_000004.10:g.63106148C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-6009C>T
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