Canonical Allele Identifier: CA2274723051
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs2047487328

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811420T>C , CM000679.2:g.73811420T>C GRCh38
NC_000017.10:g.71807559T>C , CM000679.1:g.71807559T>C GRCh37
NC_000017.9:g.69319154T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027146.1:n.228+12268A>G