Canonical Allele Identifier: CA1525089288
Gene: LINC02145 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324139G= , CM000667.2:g.6324139G= GRCh38
NC_000005.9:g.6324252G= , CM000667.1:g.6324252G= GRCh37
NC_000005.8:g.6377252G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_028351.1:n.144-11423C=