Canonical Allele Identifier: CA1099151863
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1783254171
gnomAD v3: 7-20954884-C-G
gnomAD v4: 7-20954884-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954884C>G , CM000669.2:g.20954884C>G GRCh38
NC_000007.13:g.20994503C>G , CM000669.1:g.20994503C>G GRCh37
NC_000007.12:g.20961028C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-65984C>G