Canonical Allele Identifier: CA1099151840

Gene: LINC01162

Linked Data

• dbSNP Id: rs1783253165
• gnomAD v3: 7-20954787-A-T
• gnomAD v4: 7-20954787-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20954787A>T , CM000669.2:g.20954787A>T	GRCh38
NC_000007.13:g.20994406A>T , CM000669.1:g.20994406A>T	GRCh37
NC_000007.12:g.20960931A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126381.1:n.152-66081A>T