Canonical Allele Identifier: CA836611525

Gene: LINC01162

Linked Data

• dbSNP Id: rs1482291086
• gnomAD v3: 7-20954786-T-A
• gnomAD v4: 7-20954786-T-A
• MyVariant Identifiers: chr7:g.20994405T>A (hg19) ; chr7:g.20954786T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20954786T>A , CM000669.2:g.20954786T>A	GRCh38
NC_000007.13:g.20994405T>A , CM000669.1:g.20994405T>A	GRCh37
NC_000007.12:g.20960930T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_126381.1:n.152-66082T>A