Canonical Allele Identifier: CA1693234795
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954835A= , CM000669.2:g.20954835A= GRCh38
NC_000007.13:g.20994454A= , CM000669.1:g.20994454A= GRCh37
NC_000007.12:g.20960979A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66033A=