Canonical Allele Identifier: CA1665202238
Gene: LINC01312 HGNC NCBI
TARID HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133837592G= , CM000668.2:g.133837592G= GRCh38
NC_000006.11:g.134158730G= , CM000668.1:g.134158730G= GRCh37
NC_000006.10:g.134200423G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027030.1:n.590-1G= (LINC01312)
NR_109982.1:n.478+8285C= (TARID)