Canonical Allele Identifier: CA155638056
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs13245023
gnomAD v3: 7-20845476-C-T
gnomAD v4: 7-20845476-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845476C>T , CM000669.2:g.20845476C>T GRCh38
NC_000007.13:g.20885095C>T , CM000669.1:g.20885095C>T GRCh37
NC_000007.12:g.20851620C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_126381.1:n.74+9972C>T