Canonical Allele Identifier: CA452310420

Gene: LINC01312 TARID

Linked Data

• gnomAD v4: 6-133837598-G-T
• MyVariant Identifiers: chr6:g.134158736G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133837598G>T , CM000668.2:g.133837598G>T	GRCh38
NC_000006.11:g.134158736G>T , CM000668.1:g.134158736G>T	GRCh37
NC_000006.10:g.134200429G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_027030.1:n.595G>T (LINC01312)
NR_109982.1:n.478+8279C>A (TARID)