Canonical Allele Identifier: CA214889940

Gene: LINC01153

Linked Data

• dbSNP Id: rs796491768
• gnomAD v2: 10-122939427-T-C
• gnomAD v3: 10-121179913-T-C
• gnomAD v4: 10-121179913-T-C
• MyVariant Identifiers: chr10:g.122939427T>C (hg19) ; chr10:g.121179913T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121179913T>C , CM000672.2:g.121179913T>C	GRCh38
NC_000010.10:g.122939427T>C , CM000672.1:g.122939427T>C	GRCh37
NC_000010.9:g.122929417T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_246197.2:n.684+941T>C