Canonical Allele Identifier: CA405275050
Gene: CEBPA HGNC NCBI

Linked Data

ClinVar Variation Id: 570057
ClinVar RCV Id: RCV000690829 RCV003128644
dbSNP Id: rs1300977671
gnomAD v2: 19-33792929-T-A
gnomAD v3: 19-33302023-T-A
gnomAD v4: 19-33302023-T-A
MyVariant Identifiers: chr19:g.33792929T>A (hg19) chr19:g.33302023T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33302023T>A , CM000681.2:g.33302023T>A GRCh38
NC_000019.9:g.33792929T>A , CM000681.1:g.33792929T>A GRCh37
NC_000019.8:g.38484769T>A NCBI36
NG_012022.1:g.5502A>T , LRG_456:g.5502A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.392A>T MANE Select ENSP00000427514.1:p.Tyr131Phe
ENST00000498907.2:c.392A>T ENSP00000427514.1:p.Tyr131Phe
NM_001285829.1:c.35A>T NP_001272758.1:p.Tyr12Phe
NM_001287424.1:c.497A>T NP_001274353.1:p.Tyr166Phe
NM_001287435.1:c.350A>T NP_001274364.1:p.Tyr117Phe
NM_004364.4:c.392A>T NP_004355.2:p.Tyr131Phe
NM_001287424.2:c.497A>T NP_001274353.1:p.Tyr166Phe
NM_004364.5:c.392A>T MANE Select NP_004355.2:p.Tyr131Phe
NM_001285829.2:c.35A>T NP_001272758.1:p.Tyr12Phe
NM_001287435.2:c.350A>T NP_001274364.1:p.Tyr117Phe
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