Canonical Allele Identifier: CA405275045

Gene: CEBPA

Linked Data

• ClinVar Variation Id: 2958626
• ClinVar RCV Id: RCV003816849
• gnomAD v4: 19-33302020-C-T
• MyVariant Identifiers: chr19:g.33792926C>T (hg19) ; chr19:g.33302020C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33302020C>T , CM000681.2:g.33302020C>T	GRCh38
NC_000019.9:g.33792926C>T , CM000681.1:g.33792926C>T	GRCh37
NC_000019.8:g.38484766C>T	NCBI36
NG_012022.1:g.5505G>A , LRG_456:g.5505G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000498907.3:c.395G>A MANE Select	ENSP00000427514.1:p.Gly132Asp
ENST00000498907.2:c.395G>A	ENSP00000427514.1:p.Gly132Asp
NM_001285829.1:c.38G>A	NP_001272758.1:p.Gly13Asp
NM_001287424.1:c.500G>A	NP_001274353.1:p.Gly167Asp
NM_001287435.1:c.353G>A	NP_001274364.1:p.Gly118Asp
NM_004364.4:c.395G>A	NP_004355.2:p.Gly132Asp
NM_001287424.2:c.500G>A	NP_001274353.1:p.Gly167Asp
NM_004364.5:c.395G>A MANE Select	NP_004355.2:p.Gly132Asp
NM_001285829.2:c.38G>A	NP_001272758.1:p.Gly13Asp
NM_001287435.2:c.353G>A	NP_001274364.1:p.Gly118Asp