Canonical Allele Identifier: CA506909682
Gene: CEBPA HGNC NCBI

Linked Data

dbSNP Id: rs1967117318
MyVariant Identifiers: chr19:g.33791039G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33300133G>A , CM000681.2:g.33300133G>A GRCh38
NC_000019.9:g.33791039G>A , CM000681.1:g.33791039G>A GRCh37
NC_000019.8:g.38482879G>A NCBI36
NG_012022.1:g.7392C>T , LRG_456:g.7392C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000498907.3:c.*1205C>T MANE Select ENSP00000427514.1:n.*1205C>T
ENST00000498907.2:c.*1205C>T ENSP00000427514.1:n.*1205C>T
NM_001285829.1:c.*1205C>T NP_001272758.1:n.*1205C>T
NM_001287424.1:c.*1205C>T NP_001274353.1:n.*1205C>T
NM_001287435.1:c.*1205C>T NP_001274364.1:n.*1205C>T
NM_004364.4:c.*1205C>T NP_004355.2:n.*1205C>T
NM_001287424.2:c.*1205C>T NP_001274353.1:n.*1205C>T
NM_004364.5:c.*1205C>T MANE Select NP_004355.2:n.*1205C>T
NM_001285829.2:c.*1205C>T NP_001272758.1:n.*1205C>T
NM_001287435.2:c.*1205C>T NP_001274364.1:n.*1205C>T