Canonical Allele Identifier: CA1119100822

Gene: LINC00824

Linked Data

• dbSNP Id: rs1816372946
• gnomAD v3: 8-128546932-T-C
• gnomAD v4: 8-128546932-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128546932T>C , CM000670.2:g.128546932T>C	GRCh38
NC_000008.10:g.129559178T>C , CM000670.1:g.129559178T>C	GRCh37
NC_000008.9:g.129628360T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121672.1:n.508+14138A>G