Canonical Allele Identifier: CA1869205430
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261873A= , CM000671.2:g.103261873A= GRCh38
NC_000009.11:g.106024155A= , CM000671.1:g.106024155A= GRCh37
NC_000009.10:g.105063976A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2651T=