Canonical Allele Identifier: CA1526081657
Gene: LINC02226 HGNC NCBI

Linked Data

dbSNP Id: rs1739819728
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.8439505T>C , CM000667.2:g.8439505T>C GRCh38
NC_000005.9:g.8439618T>C , CM000667.1:g.8439618T>C GRCh37
NC_000005.8:g.8492618T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_039984.1:n.174+12718A>G
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