Canonical Allele Identifier: CA197961798
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs995862979

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261921A>T , CM000671.2:g.103261921A>T GRCh38
NC_000009.11:g.106024203A>T , CM000671.1:g.106024203A>T GRCh37
NC_000009.10:g.105064024A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2603T>A