Canonical Allele Identifier: CA155651885

Gene: LINC01162

Linked Data

• dbSNP Id: rs1056499560
• gnomAD v2: 7-20994514-C-A
• gnomAD v3: 7-20954895-C-A
• gnomAD v4: 7-20954895-C-A
• MyVariant Identifiers: chr7:g.20994514C>A (hg19) ; chr7:g.20954895C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20954895C>A , CM000669.2:g.20954895C>A	GRCh38
NC_000007.13:g.20994514C>A , CM000669.1:g.20994514C>A	GRCh37
NC_000007.12:g.20961039C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_126381.1:n.152-65973C>A