Canonical Allele Identifier: CA507007840
Gene: CEBPA HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.33792931G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33302025G>T , CM000681.2:g.33302025G>T GRCh38
NC_000019.9:g.33792931G>T , CM000681.1:g.33792931G>T GRCh37
NC_000019.8:g.38484771G>T NCBI36
NG_012022.1:g.5500C>A , LRG_456:g.5500C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000498907.3:c.390C>A MANE Select ENSP00000427514.1:p.Gly130=
ENST00000498907.2:c.390C>A ENSP00000427514.1:p.Gly130=
NM_001285829.1:c.33C>A NP_001272758.1:p.Gly11=
NM_001287424.1:c.495C>A NP_001274353.1:p.Gly165=
NM_001287435.1:c.348C>A NP_001274364.1:p.Gly116=
NM_004364.4:c.390C>A NP_004355.2:p.Gly130=
NM_001287424.2:c.495C>A NP_001274353.1:p.Gly165=
NM_004364.5:c.390C>A MANE Select NP_004355.2:p.Gly130=
NM_001285829.2:c.33C>A NP_001272758.1:p.Gly11=
NM_001287435.2:c.348C>A NP_001274364.1:p.Gly116=