Canonical Allele Identifier: CA1525089315
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs1737043011

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324189C>T , CM000667.2:g.6324189C>T GRCh38
NC_000005.9:g.6324302C>T , CM000667.1:g.6324302C>T GRCh37
NC_000005.8:g.6377302C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11473G>A