Canonical Allele Identifier: CA407922171
Gene: TRIB3 HGNC NCBI

Linked Data

dbSNP Id: rs1289001951
gnomAD v2: 20-368726-C-G
gnomAD v4: 20-388082-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.388082C>G , CM000682.2:g.388082C>G GRCh38
NC_000020.10:g.368726C>G , CM000682.1:g.368726C>G GRCh37
NC_000020.9:g.316726C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000217233.9:c.72C>G MANE Select ENSP00000217233.3:p.Asn24Lys
ENST00000217233.8:c.72C>G ENSP00000217233.3:p.Asn24Lys
ENST00000217233.7:c.72C>G ENSP00000217233.3:p.Asn24Lys
ENST00000422053.3:c.153C>G ENSP00000415416.2:p.Asn51Lys
ENST00000449710.5:c.72C>G ENSP00000391873.1:p.Asn24Lys
ENST00000615226.4:c.72C>G ENSP00000478194.1:p.Asn24Lys
NM_001301188.1:c.72C>G NP_001288117.1:p.Asn24Lys
NM_001301190.1:c.72C>G NP_001288119.1:p.Asn24Lys
NM_001301193.1:c.72C>G NP_001288122.1:p.Asn24Lys
NM_001301196.1:c.72C>G NP_001288125.1:p.Asn24Lys
NM_001301201.1:c.153C>G NP_001288130.1:p.Asn51Lys
NM_021158.4:c.72C>G NP_066981.2:p.Asn24Lys
XM_017027989.2:c.153C>G XP_016883478.1:p.Asn51Lys
NM_021158.5:c.72C>G MANE Select NP_066981.2:p.Asn24Lys