Canonical Allele Identifier: CA1525089329
Gene: LINC02145 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324249G= , CM000667.2:g.6324249G= GRCh38
NC_000005.9:g.6324362G= , CM000667.1:g.6324362G= GRCh37
NC_000005.8:g.6377362G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11533C=