Canonical Allele Identifier: CA294608026
Gene: LINC00469 HGNC NCBI

Linked Data

dbSNP Id: rs941419292
gnomAD v2: 17-71807706-C-T
gnomAD v3: 17-73811567-C-T
gnomAD v4: 17-73811567-C-T
MyVariant Identifiers: chr17:g.71807706C>T (hg19) chr17:g.73811567C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73811567C>T , CM000679.2:g.73811567C>T GRCh38
NC_000017.10:g.71807706C>T , CM000679.1:g.71807706C>T GRCh37
NC_000017.9:g.69319301C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027146.1:n.228+12121G>A
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