Canonical Allele Identifier: CA197961787
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs766336314

Genomic Alleles

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

Transcript Alleles

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