Canonical Allele Identifier: CA836600957

Gene: LINC01162

Linked Data

• dbSNP Id: rs1410330599
• MyVariant Identifiers: chr7:g.20884998A>G (hg19) ; chr7:g.20845379A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20845379A>G , CM000669.2:g.20845379A>G	GRCh38
NC_000007.13:g.20884998A>G , CM000669.1:g.20884998A>G	GRCh37
NC_000007.12:g.20851523A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126381.1:n.74+9875A>G