Canonical Allele Identifier: CA653217539
Gene: LINC01492 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261862A>T , CM000671.2:g.103261862A>T GRCh38
NC_000009.11:g.106024144A>T , CM000671.1:g.106024144A>T GRCh37
NC_000009.10:g.105063965A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2662T>A