Canonical Allele Identifier: CA1869205482
Gene: LINC01492 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261995C= , CM000671.2:g.103261995C= GRCh38
NC_000009.11:g.106024277C= , CM000671.1:g.106024277C= GRCh37
NC_000009.10:g.105064098C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2529G=