Canonical Allele Identifier: CA296568472
Gene:

Linked Data

dbSNP Id: rs972583587
gnomAD v2: 18-10321419-C-T
gnomAD v3: 18-10321422-C-T
gnomAD v4: 18-10321422-C-T
MyVariant Identifiers: chr18:g.10321419C>T (hg19) chr18:g.10321422C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321422C>T , CM000680.2:g.10321422C>T GRCh38
NC_000018.9:g.10321419C>T , CM000680.1:g.10321419C>T GRCh37
NC_000018.8:g.10311419C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+726G>A
XR_001753344.1:n.650+726G>A
XR_001753345.1:n.699G>A
XR_001753346.1:n.549+726G>A
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