Canonical Allele Identifier: CA197961785
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs748593329

Genomic Alleles

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

Transcript Alleles

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