Canonical Allele Identifier: CA296576135

Gene:

Linked Data

• dbSNP Id: rs1009954612
• gnomAD v3: 18-10382799-T-C
• gnomAD v4: 18-10382799-T-C
• MyVariant Identifiers: chr18:g.10382796T>C (hg19) ; chr18:g.10382799T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10382799T>C , CM000680.2:g.10382799T>C	GRCh38
NC_000018.9:g.10382796T>C , CM000680.1:g.10382796T>C	GRCh37
NC_000018.8:g.10372796T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_935143.1:n.919+1446T>C