Canonical Allele Identifier: CA1968512934
Gene:

Linked Data

dbSNP Id: rs1856777894
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506503G>A , CM000673.2:g.45506503G>A GRCh38
NC_000011.9:g.45528053G>A , CM000673.1:g.45528053G>A GRCh37
NC_000011.8:g.45484629G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16732C>T
XR_931245.3:n.566-16732C>T
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