Canonical Allele Identifier: CA296568444
Gene:

Linked Data

dbSNP Id: rs1025835057
gnomAD v3: 18-10321220-C-T
gnomAD v4: 18-10321220-C-T
MyVariant Identifiers: chr18:g.10321217C>T (hg19) chr18:g.10321220C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321220C>T , CM000680.2:g.10321220C>T GRCh38
NC_000018.9:g.10321217C>T , CM000680.1:g.10321217C>T GRCh37
NC_000018.8:g.10311217C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+928G>A
XR_001753344.1:n.650+928G>A
XR_001753345.1:n.901G>A
XR_001753346.1:n.549+928G>A
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