Canonical Allele Identifier: CA1576425802
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs1753178649
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365690A>G , CM000667.2:g.118365690A>G GRCh38
NC_000005.9:g.117701385A>G , CM000667.1:g.117701385A>G GRCh37
NC_000005.8:g.117729284A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14183T>C
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