Canonical Allele Identifier: CA9722496

Gene: TRIB3

Linked Data

• ClinVar Variation Id: 710947
• ClinVar RCV Id: RCV000882628
• dbSNP Id: rs56092421
• ExAC: 20:368735 C / T
• gnomAD v2: 20-368735-C-T
• gnomAD v3: 20-388091-C-T
• gnomAD v4: 20-388091-C-T
• MyVariant Identifiers: chr20:g.368735C>T (hg19) ; chr20:g.388091C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.388091C>T , CM000682.2:g.388091C>T	GRCh38
NC_000020.10:g.368735C>T , CM000682.1:g.368735C>T	GRCh37
NC_000020.9:g.316735C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217233.9:c.81C>T MANE Select	ENSP00000217233.3:p.Thr27=
ENST00000217233.8:c.81C>T	ENSP00000217233.3:p.Thr27=
ENST00000217233.7:c.81C>T	ENSP00000217233.3:p.Thr27=
ENST00000422053.3:c.162C>T	ENSP00000415416.2:p.Thr54=
ENST00000449710.5:c.81C>T	ENSP00000391873.1:p.Thr27=
ENST00000615226.4:c.81C>T	ENSP00000478194.1:p.Thr27=
NM_001301188.1:c.81C>T	NP_001288117.1:p.Thr27=
NM_001301190.1:c.81C>T	NP_001288119.1:p.Thr27=
NM_001301193.1:c.81C>T	NP_001288122.1:p.Thr27=
NM_001301196.1:c.81C>T	NP_001288125.1:p.Thr27=
NM_001301201.1:c.162C>T	NP_001288130.1:p.Thr54=
NM_021158.4:c.81C>T	NP_066981.2:p.Thr27=
XM_017027989.2:c.162C>T	XP_016883478.1:p.Thr54=
NM_021158.5:c.81C>T MANE Select	NP_066981.2:p.Thr27=