Canonical Allele Identifier: CA781419128

Gene: LINC01924

Linked Data

• dbSNP Id: rs1191746358
• gnomAD v3: 18-64209762-CT-C
• gnomAD v4: 18-64209762-CT-C
• MyVariant Identifiers: chr18:g.61876998del (hg19) ; chr18:g.64209763del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.64209763del , CM000680.2:g.64209763del	GRCh38
NC_000018.9:g.61876998del , CM000680.1:g.61876998del	GRCh37
NC_000018.8:g.60027978del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033881.1:n.201-39538del