Canonical Allele Identifier: CA2274723127
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs2047488167

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811548A>G , CM000679.2:g.73811548A>G GRCh38
NC_000017.10:g.71807687A>G , CM000679.1:g.71807687A>G GRCh37
NC_000017.9:g.69319282A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027146.1:n.228+12140T>C