Canonical Allele Identifier: CA1099151876
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1783254573
gnomAD v3: 7-20954915-A-G
gnomAD v4: 7-20954915-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954915A>G , CM000669.2:g.20954915A>G GRCh38
NC_000007.13:g.20994534A>G , CM000669.1:g.20994534A>G GRCh37
NC_000007.12:g.20961059A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_126381.1:n.152-65953A>G
Search 100 bp 5'
Search 100 bp 3'