Canonical Allele Identifier: CA1665202227
Gene: LINC01312 HGNC NCBI
TARID HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133837572_133837573delinsCT , CM000668.2:g.133837572_133837573delinsCT GRCh38
NC_000006.11:g.134158710_134158711delinsCT , CM000668.1:g.134158710_134158711delinsCT GRCh37
NC_000006.10:g.134200403_134200404delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027030.1:n.590-21_590-20delinsCT (LINC01312)
NR_109982.1:n.478+8304_478+8305delinsAG (TARID)