Canonical Allele Identifier: CA452310411
Gene: LINC01312 HGNC NCBI
TARID HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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