Canonical Allele Identifier: CA1693234738
Gene: LINC01162 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954786_20954787delinsTA , CM000669.2:g.20954786_20954787delinsTA GRCh38
NC_000007.13:g.20994405_20994406delinsTA , CM000669.1:g.20994405_20994406delinsTA GRCh37
NC_000007.12:g.20960930_20960931delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_126381.1:n.152-66082_152-66081delinsTA
Search 100 bp 5'
Search 100 bp 3'