Canonical Allele Identifier: CA991159729

Gene: LINC01924

Linked Data

• dbSNP Id: rs2051785919
• gnomAD v3: 18-64209757-C-T
• gnomAD v4: 18-64209757-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.64209757C>T , CM000680.2:g.64209757C>T	GRCh38
NC_000018.9:g.61876992C>T , CM000680.1:g.61876992C>T	GRCh37
NC_000018.8:g.60027972C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033881.1:n.201-39544C>T