Canonical Allele Identifier: CA296568438

Gene:

Linked Data

• dbSNP Id: rs543153398
• gnomAD v3: 18-10321190-C-T
• gnomAD v4: 18-10321190-C-T
• MyVariant Identifiers: chr18:g.10321187C>T (hg19) ; chr18:g.10321190C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10321190C>T , CM000680.2:g.10321190C>T	GRCh38
NC_000018.9:g.10321187C>T , CM000680.1:g.10321187C>T	GRCh37
NC_000018.8:g.10311187C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935138.1:n.665+958G>A
XR_001753344.1:n.650+958G>A
XR_001753345.1:n.931G>A
XR_001753346.1:n.549+958G>A