Canonical Allele Identifier: CA405275039

Gene: CEBPA

Linked Data

• gnomAD v4: 19-33302017-C-G
• MyVariant Identifiers: chr19:g.33792923C>G (hg19) ; chr19:g.33302017C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33302017C>G , CM000681.2:g.33302017C>G	GRCh38
NC_000019.9:g.33792923C>G , CM000681.1:g.33792923C>G	GRCh37
NC_000019.8:g.38484763C>G	NCBI36
NG_012022.1:g.5508G>C , LRG_456:g.5508G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000498907.3:c.398G>C MANE Select	ENSP00000427514.1:p.Cys133Ser
ENST00000498907.2:c.398G>C	ENSP00000427514.1:p.Cys133Ser
NM_001285829.1:c.41G>C	NP_001272758.1:p.Cys14Ser
NM_001287424.1:c.503G>C	NP_001274353.1:p.Cys168Ser
NM_001287435.1:c.356G>C	NP_001274364.1:p.Cys119Ser
NM_004364.4:c.398G>C	NP_004355.2:p.Cys133Ser
NM_001287424.2:c.503G>C	NP_001274353.1:p.Cys168Ser
NM_004364.5:c.398G>C MANE Select	NP_004355.2:p.Cys133Ser
NM_001285829.2:c.41G>C	NP_001272758.1:p.Cys14Ser
NM_001287435.2:c.356G>C	NP_001274364.1:p.Cys119Ser