Canonical Allele Identifier: CA776019152

Gene:

Linked Data

• dbSNP Id: rs1241412417
• gnomAD v3: 18-10382793-G-A
• gnomAD v4: 18-10382793-G-A
• MyVariant Identifiers: chr18:g.10382790G>A (hg19) ; chr18:g.10382793G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10382793G>A , CM000680.2:g.10382793G>A	GRCh38
NC_000018.9:g.10382790G>A , CM000680.1:g.10382790G>A	GRCh37
NC_000018.8:g.10372790G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_935143.1:n.919+1440G>A