Canonical Allele Identifier: CA298296899

Gene:

Linked Data

• dbSNP Id: rs557452670
• gnomAD v2: 18-29337026-A-G
• gnomAD v3: 18-31757063-A-G
• gnomAD v4: 18-31757063-A-G
• MyVariant Identifiers: chr18:g.29337026A>G (hg19) ; chr18:g.31757063A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31757063A>G , CM000680.2:g.31757063A>G	GRCh38
NC_000018.9:g.29337026A>G , CM000680.1:g.29337026A>G	GRCh37
NC_000018.8:g.27591024A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5076A>G