Canonical Allele Identifier: CA1050454519
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1704111410
gnomAD v3: 3-86495339-A-C
gnomAD v4: 3-86495339-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495339A>C , CM000665.2:g.86495339A>C GRCh38
NC_000003.11:g.86544489A>C , CM000665.1:g.86544489A>C GRCh37
NC_000003.10:g.86627179A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-452A>C
NR_135563.1:n.116-452A>C