Canonical Allele Identifier: CA126242383
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs933315316
MyVariant Identifiers: chr5:g.117701401A>C (hg19) chr5:g.118365706A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365706A>C , CM000667.2:g.118365706A>C GRCh38
NC_000005.9:g.117701401A>C , CM000667.1:g.117701401A>C GRCh37
NC_000005.8:g.117729300A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14199T>G
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