Canonical Allele Identifier: CA972306045
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs1416957254
gnomAD v3: 15-85756812-T-G
gnomAD v4: 15-85756812-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756812T>G , CM000677.2:g.85756812T>G GRCh38
NC_000015.9:g.86300043T>G , CM000677.1:g.86300043T>G GRCh37
NC_000015.8:g.84101047T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120366.1:n.420-856A>C
Search 100 bp 5'
Search 100 bp 3'