Canonical Allele Identifier: CA1869205542
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262105_103262106delinsTG , CM000671.2:g.103262105_103262106delinsTG GRCh38
NC_000009.11:g.106024387_106024388delinsTG , CM000671.1:g.106024387_106024388delinsTG GRCh37
NC_000009.10:g.105064208_105064209delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2418_771+2419delinsCA