Canonical Allele Identifier: CA506910456

Gene: CEBPA

Linked Data

• dbSNP Id: rs1600018718
• gnomAD v4: 19-33300399-A-G
• MyVariant Identifiers: chr19:g.33791305A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33300399A>G , CM000681.2:g.33300399A>G	GRCh38
NC_000019.9:g.33791305A>G , CM000681.1:g.33791305A>G	GRCh37
NC_000019.8:g.38483145A>G	NCBI36
NG_012022.1:g.7126T>C , LRG_456:g.7126T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.*939T>C MANE Select	ENSP00000427514.1:n.*939T>C
ENST00000498907.2:c.*939T>C	ENSP00000427514.1:n.*939T>C
NM_001285829.1:c.*939T>C	NP_001272758.1:n.*939T>C
NM_001287424.1:c.*939T>C	NP_001274353.1:n.*939T>C
NM_001287435.1:c.*939T>C	NP_001274364.1:n.*939T>C
NM_004364.4:c.*939T>C	NP_004355.2:n.*939T>C
NM_001287424.2:c.*939T>C	NP_001274353.1:n.*939T>C
NM_004364.5:c.*939T>C MANE Select	NP_004355.2:n.*939T>C
NM_001285829.2:c.*939T>C	NP_001272758.1:n.*939T>C
NM_001287435.2:c.*939T>C	NP_001274364.1:n.*939T>C