Canonical Allele Identifier: CA809186601
Gene: LINC02211 HGNC NCBI

Linked Data

dbSNP Id: rs1179945222
gnomAD v3: 5-25420020-T-C
gnomAD v4: 5-25420020-T-C
MyVariant Identifiers: chr5:g.25420129T>C (hg19) chr5:g.25420020T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.25420020T>C , CM000667.2:g.25420020T>C GRCh38
NC_000005.9:g.25420129T>C , CM000667.1:g.25420129T>C GRCh37
NC_000005.8:g.25455886T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011514196.1:c.*59+63922T>C XP_011512498.1:n.*59+63922T>C
Search 100 bp 5'
Search 100 bp 3'