Canonical Allele Identifier: CA1869205423
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs371055467

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261860G>A , CM000671.2:g.103261860G>A GRCh38
NC_000009.11:g.106024142G>A , CM000671.1:g.106024142G>A GRCh37
NC_000009.10:g.105063963G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2664C>T