Canonical Allele Identifier: CA1525089333
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs1737043744

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324252A>T , CM000667.2:g.6324252A>T GRCh38
NC_000005.9:g.6324365A>T , CM000667.1:g.6324365A>T GRCh37
NC_000005.8:g.6377365A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11536T>A