Canonical Allele Identifier: CA776019226

Gene:

Linked Data

• dbSNP Id: rs1338169180
• gnomAD v3: 18-10382899-C-T
• gnomAD v4: 18-10382899-C-T
• MyVariant Identifiers: chr18:g.10382896C>T (hg19) ; chr18:g.10382899C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10382899C>T , CM000680.2:g.10382899C>T	GRCh38
NC_000018.9:g.10382896C>T , CM000680.1:g.10382896C>T	GRCh37
NC_000018.8:g.10372896C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_935143.1:n.919+1546C>T