Canonical Allele Identifier: CA296568448
Gene:

Linked Data

dbSNP Id: rs1013800081
gnomAD v2: 18-10321237-C-A
gnomAD v3: 18-10321240-C-A
gnomAD v4: 18-10321240-C-A
MyVariant Identifiers: chr18:g.10321237C>A (hg19) chr18:g.10321240C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321240C>A , CM000680.2:g.10321240C>A GRCh38
NC_000018.9:g.10321237C>A , CM000680.1:g.10321237C>A GRCh37
NC_000018.8:g.10311237C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+908G>T
XR_001753344.1:n.650+908G>T
XR_001753345.1:n.881G>T
XR_001753346.1:n.549+908G>T
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