Canonical Allele Identifier: CA2712947172
Gene: LINC01312 HGNC NCBI
TARID HGNC NCBI

Linked Data

dbSNP Id: rs2114497184

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133837584T>C , CM000668.2:g.133837584T>C GRCh38
NC_000006.11:g.134158722T>C , CM000668.1:g.134158722T>C GRCh37
NC_000006.10:g.134200415T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027030.1:n.590-9T>C (LINC01312)
NR_109982.1:n.478+8293A>G (TARID)