Canonical Allele Identifier: CA155651876
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs985919541
MyVariant Identifiers: chr7:g.20994446G>A (hg19) chr7:g.20954827G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954827G>A , CM000669.2:g.20954827G>A GRCh38
NC_000007.13:g.20994446G>A , CM000669.1:g.20994446G>A GRCh37
NC_000007.12:g.20960971G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66041G>A
Search 100 bp 5'
Search 100 bp 3'