Canonical Allele Identifier: CA11963850
Gene: LINC02211 HGNC NCBI

Linked Data

dbSNP Id: rs1904173
gnomAD v2: 5-25420089-G-A
gnomAD v3: 5-25419980-G-A
gnomAD v4: 5-25419980-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.25419980G>A , CM000667.2:g.25419980G>A GRCh38
NC_000005.9:g.25420089G>A , CM000667.1:g.25420089G>A GRCh37
NC_000005.8:g.25455846G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011514196.1:c.*59+63882G>A XP_011512498.1:n.*59+63882G>A