Canonical Allele Identifier: CA2571778151
Gene: LINC02145 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324187T>C , CM000667.2:g.6324187T>C GRCh38
NC_000005.9:g.6324300T>C , CM000667.1:g.6324300T>C GRCh37
NC_000005.8:g.6377300T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_028351.1:n.144-11471A>G