Canonical Allele Identifier: CA857924178
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1299162205

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261850A>G , CM000671.2:g.103261850A>G GRCh38
NC_000009.11:g.106024132A>G , CM000671.1:g.106024132A>G GRCh37
NC_000009.10:g.105063953A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121578.1:n.771+2674T>C