Canonical Allele Identifier: CA506910332
Gene: CEBPA HGNC NCBI

Linked Data

dbSNP Id: rs1967122508
gnomAD v4: 19-33300356-C-T
MyVariant Identifiers: chr19:g.33791262C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33300356C>T , CM000681.2:g.33300356C>T GRCh38
NC_000019.9:g.33791262C>T , CM000681.1:g.33791262C>T GRCh37
NC_000019.8:g.38483102C>T NCBI36
NG_012022.1:g.7169G>A , LRG_456:g.7169G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.*982G>A MANE Select ENSP00000427514.1:n.*982G>A
ENST00000498907.2:c.*982G>A ENSP00000427514.1:n.*982G>A
NM_001285829.1:c.*982G>A NP_001272758.1:n.*982G>A
NM_001287424.1:c.*982G>A NP_001274353.1:n.*982G>A
NM_001287435.1:c.*982G>A NP_001274364.1:n.*982G>A
NM_004364.4:c.*982G>A NP_004355.2:n.*982G>A
NM_001287424.2:c.*982G>A NP_001274353.1:n.*982G>A
NM_004364.5:c.*982G>A MANE Select NP_004355.2:n.*982G>A
NM_001285829.2:c.*982G>A NP_001272758.1:n.*982G>A
NM_001287435.2:c.*982G>A NP_001274364.1:n.*982G>A
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