Canonical Allele Identifier: CA1050454565
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1704111730
gnomAD v3: 3-86495381-T-C
gnomAD v4: 3-86495381-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495381T>C , CM000665.2:g.86495381T>C GRCh38
NC_000003.11:g.86544531T>C , CM000665.1:g.86544531T>C GRCh37
NC_000003.10:g.86627221T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-410T>C
NR_135563.1:n.116-410T>C