Canonical Allele Identifier: CA509324479
Gene: TRIB3 HGNC NCBI

Linked Data

gnomAD v4: 20-388262-G-A
MyVariant Identifiers: chr20:g.368906G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.388262G>A , CM000682.2:g.388262G>A GRCh38
NC_000020.10:g.368906G>A , CM000682.1:g.368906G>A GRCh37
NC_000020.9:g.316906G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000217233.9:c.252G>A MANE Select ENSP00000217233.3:p.Gln84=
ENST00000217233.8:c.252G>A ENSP00000217233.3:p.Gln84=
ENST00000217233.7:c.252G>A ENSP00000217233.3:p.Gln84=
ENST00000422053.3:c.333G>A ENSP00000415416.2:p.Gln111=
ENST00000449710.5:c.252G>A ENSP00000391873.1:p.Gln84=
ENST00000615226.4:c.252G>A ENSP00000478194.1:p.Gln84=
NM_001301188.1:c.252G>A NP_001288117.1:p.Gln84=
NM_001301190.1:c.252G>A NP_001288119.1:p.Gln84=
NM_001301193.1:c.252G>A NP_001288122.1:p.Gln84=
NM_001301196.1:c.252G>A NP_001288125.1:p.Gln84=
NM_001301201.1:c.333G>A NP_001288130.1:p.Gln111=
NM_021158.4:c.252G>A NP_066981.2:p.Gln84=
XM_017027989.2:c.333G>A XP_016883478.1:p.Gln111=
NM_021158.5:c.252G>A MANE Select NP_066981.2:p.Gln84=