Canonical Allele Identifier: CA776019740

Gene:

Linked Data

• dbSNP Id: rs1260257793
• gnomAD v3: 18-10321269-C-T
• gnomAD v4: 18-10321269-C-T
• MyVariant Identifiers: chr18:g.10321266C>T (hg19) ; chr18:g.10321269C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10321269C>T , CM000680.2:g.10321269C>T	GRCh38
NC_000018.9:g.10321266C>T , CM000680.1:g.10321266C>T	GRCh37
NC_000018.8:g.10311266C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935138.1:n.665+879G>A
XR_001753344.1:n.650+879G>A
XR_001753345.1:n.852G>A
XR_001753346.1:n.549+879G>A