Canonical Allele Identifier: CA778454284
Gene:

Linked Data

dbSNP Id: rs1331026898
MyVariant Identifiers: chr18:g.29336822C>A (hg19) chr18:g.31756859C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756859C>A , CM000680.2:g.31756859C>A GRCh38
NC_000018.9:g.29336822C>A , CM000680.1:g.29336822C>A GRCh37
NC_000018.8:g.27590820C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5280C>A
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