Canonical Allele Identifier: CA1693234853
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954881C= , CM000669.2:g.20954881C= GRCh38
NC_000007.13:g.20994500C= , CM000669.1:g.20994500C= GRCh37
NC_000007.12:g.20961025C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_126381.1:n.152-65987C=