Canonical Allele Identifier: CA1869205470
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261954A= , CM000671.2:g.103261954A= GRCh38
NC_000009.11:g.106024236A= , CM000671.1:g.106024236A= GRCh37
NC_000009.10:g.105064057A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2570T=