Canonical Allele Identifier: CA1050454192
Gene: LINC02070 HGNC NCBI

Linked Data

gnomAD v3: 3-86495296-T-G
gnomAD v4: 3-86495296-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495296T>G , CM000665.2:g.86495296T>G GRCh38
NC_000003.11:g.86544446T>G , CM000665.1:g.86544446T>G GRCh37
NC_000003.10:g.86627136T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-495T>G
NR_135563.1:n.116-495T>G