Canonical Allele Identifier: CA405275255

Gene: CEBPA

Linked Data

• gnomAD v4: 19-33302123-T-A
• MyVariant Identifiers: chr19:g.33793029T>A (hg19) ; chr19:g.33302123T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33302123T>A , CM000681.2:g.33302123T>A	GRCh38
NC_000019.9:g.33793029T>A , CM000681.1:g.33793029T>A	GRCh37
NC_000019.8:g.38484869T>A	NCBI36
NG_012022.1:g.5402A>T , LRG_456:g.5402A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.292A>T MANE Select	ENSP00000427514.1:p.Thr98Ser
ENST00000498907.2:c.292A>T	ENSP00000427514.1:p.Thr98Ser
NM_001285829.1:c.-66A>T	NP_001272758.1:n.-66A>T
NM_001287424.1:c.397A>T	NP_001274353.1:p.Thr133Ser
NM_001287435.1:c.250A>T	NP_001274364.1:p.Thr84Ser
NM_004364.4:c.292A>T	NP_004355.2:p.Thr98Ser
NM_001287424.2:c.397A>T	NP_001274353.1:p.Thr133Ser
NM_004364.5:c.292A>T MANE Select	NP_004355.2:p.Thr98Ser
NM_001285829.2:c.-66A>T	NP_001272758.1:n.-66A>T
NM_001287435.2:c.250A>T	NP_001274364.1:p.Thr84Ser