Canonical Allele Identifier: CA302041024

Gene: LINC01924

Linked Data

• dbSNP Id: rs113343010
• gnomAD v3: 18-64209762-C-G
• gnomAD v4: 18-64209762-C-G
• MyVariant Identifiers: chr18:g.61876997C>G (hg19) ; chr18:g.64209762C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.64209762C>G , CM000680.2:g.64209762C>G	GRCh38
NC_000018.9:g.61876997C>G , CM000680.1:g.61876997C>G	GRCh37
NC_000018.8:g.60027977C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033881.1:n.201-39539C>G