Canonical Allele Identifier: CA1080647913
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs1753180977
gnomAD v3: 5-118365796-C-G
gnomAD v4: 5-118365796-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365796C>G , CM000667.2:g.118365796C>G GRCh38
NC_000005.9:g.117701491C>G , CM000667.1:g.117701491C>G GRCh37
NC_000005.8:g.117729390C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14289G>C
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