Canonical Allele Identifier: CA774933204

Gene: LINC00469

Linked Data

• dbSNP Id: rs1402157645
• MyVariant Identifiers: chr17:g.71807759A>G (hg19) ; chr17:g.73811620A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73811620A>G , CM000679.2:g.73811620A>G	GRCh38
NC_000017.10:g.71807759A>G , CM000679.1:g.71807759A>G	GRCh37
NC_000017.9:g.69319354A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_027146.1:n.228+12068T>C