Canonical Allele Identifier: CA15578131
Gene: LINC02055 HGNC NCBI

Linked Data

dbSNP Id: rs16906415
gnomAD v2: 8-137850011-A-G
gnomAD v3: 8-136837768-A-G
gnomAD v4: 8-136837768-A-G
MyVariant Identifiers: chr8:g.137850011A>G (hg19) chr8:g.136837768A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.136837768A>G , CM000670.2:g.136837768A>G GRCh38
NC_000008.10:g.137850011A>G , CM000670.1:g.137850011A>G GRCh37
NC_000008.9:g.137919193A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147196.1:n.443+40398A>G
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