Canonical Allele Identifier: CA307843610

Gene: CEBPA

Linked Data

• dbSNP Id: rs35196724
• MyVariant Identifiers: chr19:g.33790928C>G (hg19) ; chr19:g.33300022C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33300022C>G , CM000681.2:g.33300022C>G	GRCh38
NC_000019.9:g.33790928C>G , CM000681.1:g.33790928C>G	GRCh37
NC_000019.8:g.38482768C>G	NCBI36
NG_012022.1:g.7503G>C , LRG_456:g.7503G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.*1316G>C MANE Select	ENSP00000427514.1:n.*1316G>C
ENST00000498907.2:c.*1316G>C	ENSP00000427514.1:n.*1316G>C
NM_001285829.1:c.*1316G>C	NP_001272758.1:n.*1316G>C
NM_001287424.1:c.*1316G>C	NP_001274353.1:n.*1316G>C
NM_001287435.1:c.*1316G>C	NP_001274364.1:n.*1316G>C
NM_004364.4:c.*1316G>C	NP_004355.2:n.*1316G>C
NM_001287424.2:c.*1316G>C	NP_001274353.1:n.*1316G>C
NM_004364.5:c.*1316G>C MANE Select	NP_004355.2:n.*1316G>C
NM_001285829.2:c.*1316G>C	NP_001272758.1:n.*1316G>C
NM_001287435.2:c.*1316G>C	NP_001274364.1:n.*1316G>C