Canonical Allele Identifier: CA214889941

Gene: LINC01153

Linked Data

• dbSNP Id: rs998748565
• gnomAD v2: 10-122939429-A-C
• gnomAD v3: 10-121179915-A-C
• gnomAD v4: 10-121179915-A-C
• MyVariant Identifiers: chr10:g.122939429A>C (hg19) ; chr10:g.121179915A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121179915A>C , CM000672.2:g.121179915A>C	GRCh38
NC_000010.10:g.122939429A>C , CM000672.1:g.122939429A>C	GRCh37
NC_000010.9:g.122929419A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_246197.2:n.684+943A>C