Canonical Allele Identifier: CA155638044

Gene: LINC01162

Linked Data

• dbSNP Id: rs918272291
• gnomAD v3: 7-20845377-G-A
• gnomAD v4: 7-20845377-G-A
• MyVariant Identifiers: chr7:g.20884996G>A (hg19) ; chr7:g.20845377G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20845377G>A , CM000669.2:g.20845377G>A	GRCh38
NC_000007.13:g.20884996G>A , CM000669.1:g.20884996G>A	GRCh37
NC_000007.12:g.20851521G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126381.1:n.74+9873G>A