Canonical Allele Identifier: CA2544997719
Gene: LINC01162 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954807_20954808insTTTCTAA , CM000669.2:g.20954807_20954808insTTTCTAA GRCh38
NC_000007.13:g.20994426_20994427insTTTCTAA , CM000669.1:g.20994426_20994427insTTTCTAA GRCh37
NC_000007.12:g.20960951_20960952insTTTCTAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66061_152-66060insTTTCTAA