Canonical Allele Identifier: CA2581466864
Gene: LINC02145 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324180A>C , CM000667.2:g.6324180A>C GRCh38
NC_000005.9:g.6324293A>C , CM000667.1:g.6324293A>C GRCh37
NC_000005.8:g.6377293A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11464T>G