Canonical Allele Identifier: CA1797599582

Gene: LINC02235

Linked Data

• dbSNP Id: rs67666182

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.81859802A>T , CM000670.2:g.81859802A>T	GRCh38
NC_000008.10:g.82772037A>T , CM000670.1:g.82772037A>T	GRCh37
NC_000008.9:g.82934592A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_170313.1:n.54-13600A>T
NR_170314.1:n.223+10695A>T
NR_170315.1:n.273-13600A>T
NR_170316.1:n.360+5966A>T
NR_170317.1:n.481+5966A>T
NR_170318.1:n.755+5966A>T
NR_170319.1:n.54-3607A>T
NR_170320.1:n.616-3607A>T