Canonical Allele Identifier: CA1869205391
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1827340068

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261787A>C , CM000671.2:g.103261787A>C GRCh38
NC_000009.11:g.106024069A>C , CM000671.1:g.106024069A>C GRCh37
NC_000009.10:g.105063890A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2737T>G