Canonical Allele Identifier: CA774933229
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs1460379770
MyVariant Identifiers: chr17:g.71807783A>G (hg19) chr17:g.73811644A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811644A>G , CM000679.2:g.73811644A>G GRCh38
NC_000017.10:g.71807783A>G , CM000679.1:g.71807783A>G GRCh37
NC_000017.9:g.69319378A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12044T>C
Search 100 bp 5'
Search 100 bp 3'