Canonical Allele Identifier: CA148427344
Gene: LINC01312 HGNC NCBI
TARID HGNC NCBI

Linked Data

dbSNP Id: rs764262748

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133837581T>C , CM000668.2:g.133837581T>C GRCh38
NC_000006.11:g.134158719T>C , CM000668.1:g.134158719T>C GRCh37
NC_000006.10:g.134200412T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027030.1:n.590-12T>C (LINC01312)
NR_109982.1:n.478+8296A>G (TARID)