Canonical Allele Identifier: CA1869205479
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261993_103261994delinsTG , CM000671.2:g.103261993_103261994delinsTG GRCh38
NC_000009.11:g.106024275_106024276delinsTG , CM000671.1:g.106024275_106024276delinsTG GRCh37
NC_000009.10:g.105064096_105064097delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2530_771+2531delinsCA