Canonical Allele Identifier: CA15923572
Gene:

Linked Data

dbSNP Id: rs206626
gnomAD v2: 18-10321347-A-G
gnomAD v3: 18-10321350-A-G
gnomAD v4: 18-10321350-A-G
MyVariant Identifiers: chr18:g.10321347A>G (hg19) chr18:g.10321350A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321350A>G , CM000680.2:g.10321350A>G GRCh38
NC_000018.9:g.10321347A>G , CM000680.1:g.10321347A>G GRCh37
NC_000018.8:g.10311347A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935138.1:n.665+798T>C
XR_001753344.1:n.650+798T>C
XR_001753345.1:n.771T>C
XR_001753346.1:n.549+798T>C
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