Canonical Allele Identifier: CA2774659234
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954762A>G , CM000669.2:g.20954762A>G GRCh38
NC_000007.13:g.20994381A>G , CM000669.1:g.20994381A>G GRCh37
NC_000007.12:g.20960906A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66106A>G