Canonical Allele Identifier: CA547266977
Gene: LINC02006 HGNC NCBI

Linked Data

dbSNP Id: rs1455633849
gnomAD v2: 3-153350060-T-C
gnomAD v3: 3-153632271-T-C
gnomAD v4: 3-153632271-T-C
MyVariant Identifiers: chr3:g.153350060T>C (hg19) chr3:g.153632271T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.153632271T>C , CM000665.2:g.153632271T>C GRCh38
NC_000003.11:g.153350060T>C , CM000665.1:g.153350060T>C GRCh37
NC_000003.10:g.154832750T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924593.1:n.363-27526A>G
XR_924594.1:n.60+25799A>G
NR_146713.1:n.161-27526A>G
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