Canonical Allele Identifier: CA836600928

Gene: LINC01162

Linked Data

• dbSNP Id: rs1485396088
• gnomAD v3: 7-20845333-GC-G
• gnomAD v4: 7-20845333-GC-G
• MyVariant Identifiers: chr7:g.20884953del (hg19) ; chr7:g.20845334del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20845334del , CM000669.2:g.20845334del	GRCh38
NC_000007.13:g.20884953del , CM000669.1:g.20884953del	GRCh37
NC_000007.12:g.20851478del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126381.1:n.74+9830del