Canonical Allele Identifier: CA802666084
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs1225115375
gnomAD v3: 5-118365842-A-C
gnomAD v4: 5-118365842-A-C
MyVariant Identifiers: chr5:g.117701537A>C (hg19) chr5:g.118365842A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365842A>C , CM000667.2:g.118365842A>C GRCh38
NC_000005.9:g.117701537A>C , CM000667.1:g.117701537A>C GRCh37
NC_000005.8:g.117729436A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14335T>G
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