Canonical Allele Identifier: CA16545526
Gene: LINC00469 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12451840

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811574T>C , CM000679.2:g.73811574T>C GRCh38
NC_000017.9:g.69319308T>C NCBI36
NC_000017.10:g.71807713T>C , CM000679.1:g.71807713T>C GRCh37

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12114A>G