Canonical Allele Identifier: CA1099151868
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs114964227
gnomAD v3: 7-20954892-G-C
gnomAD v4: 7-20954892-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954892G>C , CM000669.2:g.20954892G>C GRCh38
NC_000007.13:g.20994511G>C , CM000669.1:g.20994511G>C GRCh37
NC_000007.12:g.20961036G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-65976G>C