Canonical Allele Identifier: CA86186548
Gene: LINC02006 HGNC NCBI

Linked Data

dbSNP Id: rs950859779
gnomAD v2: 3-153350155-G-A
gnomAD v3: 3-153632366-G-A
gnomAD v4: 3-153632366-G-A
MyVariant Identifiers: chr3:g.153350155G>A (hg19) chr3:g.153632366G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.153632366G>A , CM000665.2:g.153632366G>A GRCh38
NC_000003.11:g.153350155G>A , CM000665.1:g.153350155G>A GRCh37
NC_000003.10:g.154832845G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924593.1:n.363-27621C>T
XR_924594.1:n.60+25704C>T
NR_146713.1:n.161-27621C>T
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