Canonical Allele Identifier: CA127456060
Gene: LINC02240 HGNC NCBI

Linked Data

dbSNP Id: rs17468244
gnomAD v2: 5-124848906-A-G
gnomAD v3: 5-125513213-A-G
gnomAD v4: 5-125513213-A-G
MyVariant Identifiers: chr5:g.124848906A>G (hg19) chr5:g.125513213A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.125513213A>G , CM000667.2:g.125513213A>G GRCh38
NC_000005.9:g.124848906A>G , CM000667.1:g.124848906A>G GRCh37
NC_000005.8:g.124876805A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109887.1:n.257-6315A>G
Search 100 bp 5'
Search 100 bp 3'