Canonical Allele Identifier: CA9722503

Gene: TRIB3

Linked Data

• ClinVar Variation Id: 2508151
• ClinVar RCV Id: RCV004283726
• dbSNP Id: rs754475678
• ExAC: 20:368755 G / A
• gnomAD v2: 20-368755-G-A
• gnomAD v3: 20-388111-G-A
• gnomAD v4: 20-388111-G-A
• MyVariant Identifiers: chr20:g.368755G>A (hg19) ; chr20:g.388111G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.388111G>A , CM000682.2:g.388111G>A	GRCh38
NC_000020.10:g.368755G>A , CM000682.1:g.368755G>A	GRCh37
NC_000020.9:g.316755G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217233.9:c.101G>A MANE Select	ENSP00000217233.3:p.Arg34Gln
ENST00000217233.8:c.101G>A	ENSP00000217233.3:p.Arg34Gln
ENST00000217233.7:c.101G>A	ENSP00000217233.3:p.Arg34Gln
ENST00000422053.3:c.182G>A	ENSP00000415416.2:p.Arg61Gln
ENST00000449710.5:c.101G>A	ENSP00000391873.1:p.Arg34Gln
ENST00000615226.4:c.101G>A	ENSP00000478194.1:p.Arg34Gln
NM_001301188.1:c.101G>A	NP_001288117.1:p.Arg34Gln
NM_001301190.1:c.101G>A	NP_001288119.1:p.Arg34Gln
NM_001301193.1:c.101G>A	NP_001288122.1:p.Arg34Gln
NM_001301196.1:c.101G>A	NP_001288125.1:p.Arg34Gln
NM_001301201.1:c.182G>A	NP_001288130.1:p.Arg61Gln
NM_021158.4:c.101G>A	NP_066981.2:p.Arg34Gln
XM_017027989.2:c.182G>A	XP_016883478.1:p.Arg61Gln
NM_021158.5:c.101G>A MANE Select	NP_066981.2:p.Arg34Gln