Canonical Allele Identifier: CA1869205530
Gene: LINC01492 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262086_103262087delinsTC , CM000671.2:g.103262086_103262087delinsTC GRCh38
NC_000009.11:g.106024368_106024369delinsTC , CM000671.1:g.106024368_106024369delinsTC GRCh37
NC_000009.10:g.105064189_105064190delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2437_771+2438delinsGA
Search 100 bp 5'
Search 100 bp 3'