Canonical Allele Identifier: CA2774659237
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954904C>G , CM000669.2:g.20954904C>G GRCh38
NC_000007.13:g.20994523C>G , CM000669.1:g.20994523C>G GRCh37
NC_000007.12:g.20961048C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-65964C>G