Canonical Allele Identifier: CA155638046

Gene: LINC01162

Linked Data

• dbSNP Id: rs756201925
• MyVariant Identifiers: chr7:g.20885007C>T (hg19) ; chr7:g.20845388C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20845388C>T , CM000669.2:g.20845388C>T	GRCh38
NC_000007.13:g.20885007C>T , CM000669.1:g.20885007C>T	GRCh37
NC_000007.12:g.20851532C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126381.1:n.74+9884C>T