Canonical Allele Identifier: CA100141904
Gene: LINC02562 HGNC NCBI

Linked Data

dbSNP Id: rs1426063
gnomAD v2: 4-76030921-A-G
gnomAD v3: 4-75105711-A-G
gnomAD v4: 4-75105711-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.75105711A>G , CM000666.2:g.75105711A>G GRCh38
NC_000004.11:g.76030921A>G , CM000666.1:g.76030921A>G GRCh37
NC_000004.10:g.76249945A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938888.1:n.236-4296T>C
XR_938889.1:n.135-4296T>C