Canonical Allele Identifier: CA405275755

Gene: CEBPA

Linked Data

• ClinVar Variation Id: 2911843
• ClinVar RCV Id: RCV003634216
• gnomAD v4: 19-33302353-C-T
• MyVariant Identifiers: chr19:g.33793259C>T (hg19) ; chr19:g.33302353C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33302353C>T , CM000681.2:g.33302353C>T	GRCh38
NC_000019.9:g.33793259C>T , CM000681.1:g.33793259C>T	GRCh37
NC_000019.8:g.38485099C>T	NCBI36
NG_012022.1:g.5172G>A , LRG_456:g.5172G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.62G>A MANE Select	ENSP00000427514.1:p.Ser21Asn
ENST00000498907.2:c.62G>A	ENSP00000427514.1:p.Ser21Asn
NM_001285829.1:c.-296G>A	NP_001272758.1:n.-296G>A
NM_001287424.1:c.167G>A	NP_001274353.1:p.Ser56Asn
NM_001287435.1:c.20G>A	NP_001274364.1:p.Ser7Asn
NM_004364.4:c.62G>A	NP_004355.2:p.Ser21Asn
NM_001287424.2:c.167G>A	NP_001274353.1:p.Ser56Asn
NM_004364.5:c.62G>A MANE Select	NP_004355.2:p.Ser21Asn
NM_001285829.2:c.-296G>A	NP_001272758.1:n.-296G>A
NM_001287435.2:c.20G>A	NP_001274364.1:p.Ser7Asn