Canonical Allele Identifier: CA1931617888
Gene:

Linked Data

dbSNP Id: rs142304994
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100101734C>A , CM000672.2:g.100101734C>A GRCh38
NC_000010.10:g.101861491C>A , CM000672.1:g.101861491C>A GRCh37
NC_000010.9:g.101851481C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946245.1:n.185+5497C>A
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