Canonical Allele Identifier: CA1576425827
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs1753179279
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365731G>T , CM000667.2:g.118365731G>T GRCh38
NC_000005.9:g.117701426G>T , CM000667.1:g.117701426G>T GRCh37
NC_000005.8:g.117729325G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14224C>A
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