Canonical Allele Identifier: CA452310412
Gene: LINC01312 HGNC NCBI
TARID HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.134158733A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133837595A>T , CM000668.2:g.133837595A>T GRCh38
NC_000006.11:g.134158733A>T , CM000668.1:g.134158733A>T GRCh37
NC_000006.10:g.134200426A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027030.1:n.592A>T (LINC01312)
NR_109982.1:n.478+8282T>A (TARID)