Canonical Allele Identifier: CA836600966

Gene: LINC01162

Linked Data

• dbSNP Id: rs1418715934
• MyVariant Identifiers: chr7:g.20885030C>A (hg19) ; chr7:g.20845411C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20845411C>A , CM000669.2:g.20845411C>A	GRCh38
NC_000007.13:g.20885030C>A , CM000669.1:g.20885030C>A	GRCh37
NC_000007.12:g.20851555C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126381.1:n.74+9907C>A