Canonical Allele Identifier: CA741127749

Gene: LINC02871

Linked Data

• dbSNP Id: rs1314857511
• gnomAD v3: 20-10869768-T-C
• gnomAD v4: 20-10869768-T-C
• MyVariant Identifiers: chr20:g.10850416T>C (hg19) ; chr20:g.10869768T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.10869768T>C , CM000682.2:g.10869768T>C	GRCh38
NC_000020.10:g.10850416T>C , CM000682.1:g.10850416T>C	GRCh37
NC_000020.9:g.10798416T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_937255.1:n.2829+2461T>C