Canonical Allele Identifier: CA630621191

Gene: LINC01924

Linked Data

• dbSNP Id: rs1358420866
• gnomAD v2: 18-61877062-T-C
• gnomAD v3: 18-64209827-T-C
• gnomAD v4: 18-64209827-T-C
• MyVariant Identifiers: chr18:g.61877062T>C (hg19) ; chr18:g.64209827T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.64209827T>C , CM000680.2:g.64209827T>C	GRCh38
NC_000018.9:g.61877062T>C , CM000680.1:g.61877062T>C	GRCh37
NC_000018.8:g.60028042T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033881.1:n.201-39474T>C