Canonical Allele Identifier: CA296568442
Gene:

Linked Data

dbSNP Id: rs554479476
gnomAD v2: 18-10321208-A-C
gnomAD v3: 18-10321211-A-C
gnomAD v4: 18-10321211-A-C
MyVariant Identifiers: chr18:g.10321208A>C (hg19) chr18:g.10321211A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321211A>C , CM000680.2:g.10321211A>C GRCh38
NC_000018.9:g.10321208A>C , CM000680.1:g.10321208A>C GRCh37
NC_000018.8:g.10311208A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+937T>G
XR_001753344.1:n.650+937T>G
XR_001753345.1:n.910T>G
XR_001753346.1:n.549+937T>G
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