Canonical Allele Identifier: CA1869205425
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261868G= , CM000671.2:g.103261868G= GRCh38
NC_000009.11:g.106024150G= , CM000671.1:g.106024150G= GRCh37
NC_000009.10:g.105063971G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2656C=