Canonical Allele Identifier: CA1665202229
Gene: LINC01312 HGNC NCBI
TARID HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133837576T= , CM000668.2:g.133837576T= GRCh38
NC_000006.11:g.134158714T= , CM000668.1:g.134158714T= GRCh37
NC_000006.10:g.134200407T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027030.1:n.590-17T= (LINC01312)
NR_109982.1:n.478+8301A= (TARID)