Canonical Allele Identifier: CA857924169
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1278545297

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261790A>T , CM000671.2:g.103261790A>T GRCh38
NC_000009.11:g.106024072A>T , CM000671.1:g.106024072A>T GRCh37
NC_000009.10:g.105063893A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2734T>A