Canonical Allele Identifier: CA506910354
Gene: CEBPA HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.33791270G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33300364G>A , CM000681.2:g.33300364G>A GRCh38
NC_000019.9:g.33791270G>A , CM000681.1:g.33791270G>A GRCh37
NC_000019.8:g.38483110G>A NCBI36
NG_012022.1:g.7161C>T , LRG_456:g.7161C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.*974C>T MANE Select ENSP00000427514.1:n.*974C>T
ENST00000498907.2:c.*974C>T ENSP00000427514.1:n.*974C>T
NM_001285829.1:c.*974C>T NP_001272758.1:n.*974C>T
NM_001287424.1:c.*974C>T NP_001274353.1:n.*974C>T
NM_001287435.1:c.*974C>T NP_001274364.1:n.*974C>T
NM_004364.4:c.*974C>T NP_004355.2:n.*974C>T
NM_001287424.2:c.*974C>T NP_001274353.1:n.*974C>T
NM_004364.5:c.*974C>T MANE Select NP_004355.2:n.*974C>T
NM_001285829.2:c.*974C>T NP_001272758.1:n.*974C>T
NM_001287435.2:c.*974C>T NP_001274364.1:n.*974C>T