Canonical Allele Identifier: CA13965351

Gene: LINC02288

Linked Data

• dbSNP Id: rs1986116
• gnomAD v2: 14-77513844-T-C
• gnomAD v3: 14-77047501-T-C
• gnomAD v4: 14-77047501-T-C
• MyVariant Identifiers: chr14:g.77513844T>C (hg19) ; chr14:g.77047501T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77047501T>C , CM000676.2:g.77047501T>C	GRCh38
NC_000014.8:g.77513844T>C , CM000676.1:g.77513844T>C	GRCh37
NC_000014.7:g.76583597T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110554.1:n.229+6224T>C