Canonical Allele Identifier: CA1869205427
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs753758098

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261872T>A , CM000671.2:g.103261872T>A GRCh38
NC_000009.11:g.106024154T>A , CM000671.1:g.106024154T>A GRCh37
NC_000009.10:g.105063975T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2652A>T