Canonical Allele Identifier: CA405275041

Gene: CEBPA

Linked Data

• dbSNP Id: rs1197023470
• gnomAD v3: 19-33302018-A-G
• gnomAD v4: 19-33302018-A-G
• MyVariant Identifiers: chr19:g.33792924A>G (hg19) ; chr19:g.33302018A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33302018A>G , CM000681.2:g.33302018A>G	GRCh38
NC_000019.9:g.33792924A>G , CM000681.1:g.33792924A>G	GRCh37
NC_000019.8:g.38484764A>G	NCBI36
NG_012022.1:g.5507T>C , LRG_456:g.5507T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.397T>C MANE Select	ENSP00000427514.1:p.Cys133Arg
ENST00000498907.2:c.397T>C	ENSP00000427514.1:p.Cys133Arg
NM_001285829.1:c.40T>C	NP_001272758.1:p.Cys14Arg
NM_001287424.1:c.502T>C	NP_001274353.1:p.Cys168Arg
NM_001287435.1:c.355T>C	NP_001274364.1:p.Cys119Arg
NM_004364.4:c.397T>C	NP_004355.2:p.Cys133Arg
NM_001287424.2:c.502T>C	NP_001274353.1:p.Cys168Arg
NM_004364.5:c.397T>C MANE Select	NP_004355.2:p.Cys133Arg
NM_001285829.2:c.40T>C	NP_001272758.1:p.Cys14Arg
NM_001287435.2:c.355T>C	NP_001274364.1:p.Cys119Arg