Canonical Allele Identifier: CA155638040

Gene: LINC01162

Linked Data

• dbSNP Id: rs927816125
• gnomAD v3: 7-20845353-T-C
• gnomAD v4: 7-20845353-T-C
• MyVariant Identifiers: chr7:g.20884972T>C (hg19) ; chr7:g.20845353T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.20845353T>C , CM000669.2:g.20845353T>C	GRCh38
NC_000007.13:g.20884972T>C , CM000669.1:g.20884972T>C	GRCh37
NC_000007.12:g.20851497T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_126381.1:n.74+9849T>C