Canonical Allele Identifier: CA836611532

Gene: LINC01162

Linked Data

• dbSNP Id: rs1162518870
• gnomAD v3: 7-20954837-C-G
• gnomAD v4: 7-20954837-C-G
• MyVariant Identifiers: chr7:g.20994456C>G (hg19) ; chr7:g.20954837C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20954837C>G , CM000669.2:g.20954837C>G	GRCh38
NC_000007.13:g.20994456C>G , CM000669.1:g.20994456C>G	GRCh37
NC_000007.12:g.20960981C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126381.1:n.152-66031C>G