Canonical Allele Identifier: CA1099137361

Gene: LINC01162

Linked Data

• dbSNP Id: rs1781822928
• gnomAD v3: 7-20845412-T-G
• gnomAD v4: 7-20845412-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20845412T>G , CM000669.2:g.20845412T>G	GRCh38
NC_000007.13:g.20885031T>G , CM000669.1:g.20885031T>G	GRCh37
NC_000007.12:g.20851556T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126381.1:n.74+9908T>G