Canonical Allele Identifier: CA562420276
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs1364978773
gnomAD v2: 5-117701536-A-G
gnomAD v3: 5-118365841-A-G
gnomAD v4: 5-118365841-A-G
MyVariant Identifiers: chr5:g.117701536A>G (hg19) chr5:g.118365841A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365841A>G , CM000667.2:g.118365841A>G GRCh38
NC_000005.9:g.117701536A>G , CM000667.1:g.117701536A>G GRCh37
NC_000005.8:g.117729435A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14334T>C
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