Canonical Allele Identifier: CA1099137354
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1781822720
gnomAD v3: 7-20845389-T-G
gnomAD v4: 7-20845389-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845389T>G , CM000669.2:g.20845389T>G GRCh38
NC_000007.13:g.20885008T>G , CM000669.1:g.20885008T>G GRCh37
NC_000007.12:g.20851533T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9885T>G