Canonical Allele Identifier: CA12642189

Gene: LINC01162

Linked Data

• dbSNP Id: rs12155172
• gnomAD v2: 7-20994491-A-G
• gnomAD v3: 7-20954872-A-G
• gnomAD v4: 7-20954872-A-G
• MyVariant Identifiers: chr7:g.20994491A>G (hg19) ; chr7:g.20954872A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20954872A>G , CM000669.2:g.20954872A>G	GRCh38
NC_000007.13:g.20994491A>G , CM000669.1:g.20994491A>G	GRCh37
NC_000007.12:g.20961016A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_126381.1:n.152-65996A>G