Canonical Allele Identifier: CA1968513055
Gene:

Linked Data

dbSNP Id: rs1856778633
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506595A>G , CM000673.2:g.45506595A>G GRCh38
NC_000011.9:g.45528145A>G , CM000673.1:g.45528145A>G GRCh37
NC_000011.8:g.45484721A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16824T>C
XR_931245.3:n.566-16824T>C
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