Canonical Allele Identifier: CA1526081697
Gene: LINC02226 HGNC NCBI

Linked Data

dbSNP Id: rs1560916705
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.8439572G>A , CM000667.2:g.8439572G>A GRCh38
NC_000005.9:g.8439685G>A , CM000667.1:g.8439685G>A GRCh37
NC_000005.8:g.8492685G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_039984.1:n.174+12651C>T
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Search 100 bp 3'