Canonical Allele Identifier: CA1525089272
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs1473063730

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324093G>C , CM000667.2:g.6324093G>C GRCh38
NC_000005.9:g.6324206G>C , CM000667.1:g.6324206G>C GRCh37
NC_000005.8:g.6377206G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11377C>G