Canonical Allele Identifier: CA2148220477
Gene: LINC02288 HGNC NCBI

Linked Data

dbSNP Id: rs1986116
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77047501T>G , CM000676.2:g.77047501T>G GRCh38
NC_000014.8:g.77513844T>G , CM000676.1:g.77513844T>G GRCh37
NC_000014.7:g.76583597T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110554.1:n.229+6224T>G
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