Canonical Allele Identifier: CA1050454395
Gene: LINC02070 HGNC NCBI

Linked Data

gnomAD v3: 3-86495312-A-T
gnomAD v4: 3-86495312-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495312A>T , CM000665.2:g.86495312A>T GRCh38
NC_000003.11:g.86544462A>T , CM000665.1:g.86544462A>T GRCh37
NC_000003.10:g.86627152A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-479A>T
NR_135563.1:n.116-479A>T