Canonical Allele Identifier: CA1869205419
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261850A= , CM000671.2:g.103261850A= GRCh38
NC_000009.11:g.106024132A= , CM000671.1:g.106024132A= GRCh37
NC_000009.10:g.105063953A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2674T=