Canonical Allele Identifier: CA509324484
Gene: TRIB3 HGNC NCBI

Linked Data

gnomAD v4: 20-388268-G-T
MyVariant Identifiers: chr20:g.368912G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.388268G>T , CM000682.2:g.388268G>T GRCh38
NC_000020.10:g.368912G>T , CM000682.1:g.368912G>T GRCh37
NC_000020.9:g.316912G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000217233.9:c.258G>T MANE Select ENSP00000217233.3:p.Leu86=
ENST00000217233.8:c.258G>T ENSP00000217233.3:p.Leu86=
ENST00000217233.7:c.258G>T ENSP00000217233.3:p.Leu86=
ENST00000422053.3:c.339G>T ENSP00000415416.2:p.Leu113=
ENST00000449710.5:c.258G>T ENSP00000391873.1:p.Leu86=
ENST00000615226.4:c.258G>T ENSP00000478194.1:p.Leu86=
NM_001301188.1:c.258G>T NP_001288117.1:p.Leu86=
NM_001301190.1:c.258G>T NP_001288119.1:p.Leu86=
NM_001301193.1:c.258G>T NP_001288122.1:p.Leu86=
NM_001301196.1:c.258G>T NP_001288125.1:p.Leu86=
NM_001301201.1:c.339G>T NP_001288130.1:p.Leu113=
NM_021158.4:c.258G>T NP_066981.2:p.Leu86=
XM_017027989.2:c.339G>T XP_016883478.1:p.Leu113=
NM_021158.5:c.258G>T MANE Select NP_066981.2:p.Leu86=