Canonical Allele Identifier: CA1381162974
Gene: LINC02070 HGNC NCBI

Linked Data

dbSNP Id: rs1704111638

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.86495367A>G , CM000665.2:g.86495367A>G GRCh38
NC_000003.11:g.86544517A>G , CM000665.1:g.86544517A>G GRCh37
NC_000003.10:g.86627207A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245082.1:n.116-424A>G
NR_135563.1:n.116-424A>G