Canonical Allele Identifier: CA294608011
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs572023392
gnomAD v2: 17-71807582-A-C
gnomAD v3: 17-73811443-A-C
gnomAD v4: 17-73811443-A-C
MyVariant Identifiers: chr17:g.71807582A>C (hg19) chr17:g.73811443A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811443A>C , CM000679.2:g.73811443A>C GRCh38
NC_000017.10:g.71807582A>C , CM000679.1:g.71807582A>C GRCh37
NC_000017.9:g.69319177A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027146.1:n.228+12245T>G
Search 100 bp 5'
Search 100 bp 3'