Canonical Allele Identifier: CA452310416
Gene: LINC01312 HGNC NCBI
TARID HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.134158735T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133837597T>C , CM000668.2:g.133837597T>C GRCh38
NC_000006.11:g.134158735T>C , CM000668.1:g.134158735T>C GRCh37
NC_000006.10:g.134200428T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027030.1:n.594T>C (LINC01312)
NR_109982.1:n.478+8280A>G (TARID)