Canonical Allele Identifier: CA298296862

Gene:

Linked Data

• dbSNP Id: rs542468164
• gnomAD v3: 18-31756702-A-G
• gnomAD v4: 18-31756702-A-G
• MyVariant Identifiers: chr18:g.29336665A>G (hg19) ; chr18:g.31756702A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31756702A>G , CM000680.2:g.31756702A>G	GRCh38
NC_000018.9:g.29336665A>G , CM000680.1:g.29336665A>G	GRCh37
NC_000018.8:g.27590663A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5437A>G