Canonical Allele Identifier: CA1693234720
Gene: LINC01162 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954774_20954775delinsAT , CM000669.2:g.20954774_20954775delinsAT GRCh38
NC_000007.13:g.20994393_20994394delinsAT , CM000669.1:g.20994393_20994394delinsAT GRCh37
NC_000007.12:g.20960918_20960919delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_126381.1:n.152-66094_152-66093delinsAT
Search 100 bp 5'
Search 100 bp 3'