Canonical Allele Identifier: CA506910798
Gene: CEBPA HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.33791424G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33300518G>C , CM000681.2:g.33300518G>C GRCh38
NC_000019.9:g.33791424G>C , CM000681.1:g.33791424G>C GRCh37
NC_000019.8:g.38483264G>C NCBI36
NG_012022.1:g.7007C>G , LRG_456:g.7007C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.*820C>G MANE Select ENSP00000427514.1:n.*820C>G
ENST00000498907.2:c.*820C>G ENSP00000427514.1:n.*820C>G
NM_001285829.1:c.*820C>G NP_001272758.1:n.*820C>G
NM_001287424.1:c.*820C>G NP_001274353.1:n.*820C>G
NM_001287435.1:c.*820C>G NP_001274364.1:n.*820C>G
NM_004364.4:c.*820C>G NP_004355.2:n.*820C>G
NM_001287424.2:c.*820C>G NP_001274353.1:n.*820C>G
NM_004364.5:c.*820C>G MANE Select NP_004355.2:n.*820C>G
NM_001285829.2:c.*820C>G NP_001272758.1:n.*820C>G
NM_001287435.2:c.*820C>G NP_001274364.1:n.*820C>G