Canonical Allele Identifier: CA619465431
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs1435320274
gnomAD v2: 15-86300119-A-C
gnomAD v3: 15-85756888-A-C
gnomAD v4: 15-85756888-A-C
MyVariant Identifiers: chr15:g.86300119A>C (hg19) chr15:g.85756888A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756888A>C , CM000677.2:g.85756888A>C GRCh38
NC_000015.9:g.86300119A>C , CM000677.1:g.86300119A>C GRCh37
NC_000015.8:g.84101123A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.420-932T>G
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