Canonical Allele Identifier: CA1869205429
Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs1827341071

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103261873A>C , CM000671.2:g.103261873A>C GRCh38
NC_000009.11:g.106024155A>C , CM000671.1:g.106024155A>C GRCh37
NC_000009.10:g.105063976A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2651T>G