Canonical Allele Identifier: CA298296843

Gene:

Linked Data

• dbSNP Id: rs1037432340
• gnomAD v2: 18-29336496-C-T
• gnomAD v3: 18-31756533-C-T
• gnomAD v4: 18-31756533-C-T
• COSMIC: COSN18882729
• MyVariant Identifiers: chr18:g.29336496C>T (hg19) ; chr18:g.31756533C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31756533C>T , CM000680.2:g.31756533C>T	GRCh38
NC_000018.9:g.29336496C>T , CM000680.1:g.29336496C>T	GRCh37
NC_000018.8:g.27590494C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5606C>T