Canonical Allele Identifier: CA986186300

Gene: LINC00469

Linked Data

• dbSNP Id: rs2047488637
• gnomAD v3: 17-73811597-T-C
• gnomAD v4: 17-73811597-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73811597T>C , CM000679.2:g.73811597T>C	GRCh38
NC_000017.10:g.71807736T>C , CM000679.1:g.71807736T>C	GRCh37
NC_000017.9:g.69319331T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_027146.1:n.228+12091A>G