Canonical Allele Identifier: CA776019223

Gene:

Linked Data

• dbSNP Id: rs1399119756
• gnomAD v3: 18-10382893-A-G
• gnomAD v4: 18-10382893-A-G
• MyVariant Identifiers: chr18:g.10382890A>G (hg19) ; chr18:g.10382893A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10382893A>G , CM000680.2:g.10382893A>G	GRCh38
NC_000018.9:g.10382890A>G , CM000680.1:g.10382890A>G	GRCh37
NC_000018.8:g.10372890A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_935143.1:n.919+1540A>G