Canonical Allele Identifier: CA1796404099
Gene:

Linked Data

dbSNP Id: rs1563550263
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.79191201G>A , CM000670.2:g.79191201G>A GRCh38
NC_000008.10:g.80103436G>A , CM000670.1:g.80103436G>A GRCh37
NC_000008.9:g.80265991G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745720.1:n.105+830G>A
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