Canonical Allele Identifier: CA155638036
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs200343899
gnomAD v2: 7-20884937-G-A
gnomAD v3: 7-20845318-G-A
gnomAD v4: 7-20845318-G-A
MyVariant Identifiers: chr7:g.20884937G>A (hg19) chr7:g.20845318G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845318G>A , CM000669.2:g.20845318G>A GRCh38
NC_000007.13:g.20884937G>A , CM000669.1:g.20884937G>A GRCh37
NC_000007.12:g.20851462G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9814G>A
Search 100 bp 5'
Search 100 bp 3'