Canonical Allele Identifier: CA1869205346
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261671A= , CM000671.2:g.103261671A= GRCh38
NC_000009.11:g.106023953A= , CM000671.1:g.106023953A= GRCh37
NC_000009.10:g.105063774A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2853T=