Canonical Allele Identifier: CA11402979
Gene: LINC02033 HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.36821489C>T
GRCh37 chr3:g.36862980C>T
gnomAD v2:
3:36862980 C / T
gnomAD v3:
3:36821489 C / T
gnomAD v4:
chr3-36821489-C-T
Joint Max Group AF 0.44203725 (AFR)
Genomes Max Group AF 0.44203725 (AFR)
Exomes Max Group AF 0.24880138 (NFE)
dbSNP:
4624519
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36821489C>T , CM000665.2:g.36821489C>T GRCh38
NC_000003.11:g.36862980C>T , CM000665.1:g.36862980C>T GRCh37
NC_000003.10:g.36837984C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940723.1:n.498-72G>A
NR_147141.1:n.106-72G>A
Search 100 bp 5'
Search 100 bp 3'