Canonical Allele Identifier: CA294608035

Gene: LINC00469

Linked Data

• dbSNP Id: rs957732073
• gnomAD v2: 17-71807741-A-C
• gnomAD v3: 17-73811602-A-C
• gnomAD v4: 17-73811602-A-C
• MyVariant Identifiers: chr17:g.71807741A>C (hg19) ; chr17:g.73811602A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73811602A>C , CM000679.2:g.73811602A>C	GRCh38
NC_000017.10:g.71807741A>C , CM000679.1:g.71807741A>C	GRCh37
NC_000017.9:g.69319336A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_027146.1:n.228+12086T>G