Canonical Allele Identifier: CA307843725

Gene: CEBPA

Linked Data

• dbSNP Id: rs1046626496
• gnomAD v2: 19-33791232-G-A
• gnomAD v3: 19-33300326-G-A
• gnomAD v4: 19-33300326-G-A
• MyVariant Identifiers: chr19:g.33791232G>A (hg19) ; chr19:g.33300326G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33300326G>A , CM000681.2:g.33300326G>A	GRCh38
NC_000019.9:g.33791232G>A , CM000681.1:g.33791232G>A	GRCh37
NC_000019.8:g.38483072G>A	NCBI36
NG_012022.1:g.7199C>T , LRG_456:g.7199C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.*1012C>T MANE Select	ENSP00000427514.1:n.*1012C>T
ENST00000498907.2:c.*1012C>T	ENSP00000427514.1:n.*1012C>T
NM_001285829.1:c.*1012C>T	NP_001272758.1:n.*1012C>T
NM_001287424.1:c.*1012C>T	NP_001274353.1:n.*1012C>T
NM_001287435.1:c.*1012C>T	NP_001274364.1:n.*1012C>T
NM_004364.4:c.*1012C>T	NP_004355.2:n.*1012C>T
NM_001287424.2:c.*1012C>T	NP_001274353.1:n.*1012C>T
NM_004364.5:c.*1012C>T MANE Select	NP_004355.2:n.*1012C>T
NM_001285829.2:c.*1012C>T	NP_001272758.1:n.*1012C>T
NM_001287435.2:c.*1012C>T	NP_001274364.1:n.*1012C>T