Canonical Allele Identifier: CA547127613
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs1290611421
gnomAD v2: 3-147935519-C-T
gnomAD v3: 3-148217732-C-T
gnomAD v4: 3-148217732-C-T
MyVariant Identifiers: chr3:g.147935519C>T (hg19) chr3:g.148217732C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217732C>T , CM000665.2:g.148217732C>T GRCh38
NC_000003.11:g.147935519C>T , CM000665.1:g.147935519C>T GRCh37
NC_000003.10:g.149418209C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2778G>A
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