Canonical Allele Identifier: CA2129379015
Gene:

Linked Data

dbSNP Id: rs1348884333
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384759C>A , CM000676.2:g.36384759C>A GRCh38
NC_000014.8:g.36853964C>A , CM000676.1:g.36853964C>A GRCh37
NC_000014.7:g.35923715C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537428.1:c.319-12400C>A XP_011535730.1:n.319-12400C>A
XR_943756.1:n.358+23663C>A
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