Canonical Allele Identifier: CA1665202249
Gene: LINC01312 HGNC NCBI
TARID HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133837599A= , CM000668.2:g.133837599A= GRCh38
NC_000006.11:g.134158737A= , CM000668.1:g.134158737A= GRCh37
NC_000006.10:g.134200430A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027030.1:n.596A= (LINC01312)
NR_109982.1:n.478+8278T= (TARID)