Canonical Allele Identifier: CA111096855
Gene: LINC02268 HGNC NCBI

Linked Data

dbSNP Id: rs948189927
MyVariant Identifiers: chr4:g.175027428A>T (hg19) chr4:g.174106277A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174106277A>T , CM000666.2:g.174106277A>T GRCh38
NC_000004.11:g.175027428A>T , CM000666.1:g.175027428A>T GRCh37
NC_000004.10:g.175264003A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125896.1:n.276-8448T>A
XR_939484.1:n.877+18638A>T
XR_939485.1:n.877+18638A>T
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