Canonical Allele Identifier: CA857924176
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1245849685

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261844G>C , CM000671.2:g.103261844G>C GRCh38
NC_000009.11:g.106024126G>C , CM000671.1:g.106024126G>C GRCh37
NC_000009.10:g.105063947G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2680C>G