Canonical Allele Identifier: CA405275048

Gene: CEBPA

Linked Data

• dbSNP Id: rs1232538136
• MyVariant Identifiers: chr19:g.33792928G>C (hg19) ; chr19:g.33302022G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33302022G>C , CM000681.2:g.33302022G>C	GRCh38
NC_000019.9:g.33792928G>C , CM000681.1:g.33792928G>C	GRCh37
NC_000019.8:g.38484768G>C	NCBI36
NG_012022.1:g.5503C>G , LRG_456:g.5503C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.393C>G MANE Select	ENSP00000427514.1:p.Tyr131Ter
ENST00000498907.2:c.393C>G	ENSP00000427514.1:p.Tyr131Ter
NM_001285829.1:c.36C>G	NP_001272758.1:p.Tyr12Ter
NM_001287424.1:c.498C>G	NP_001274353.1:p.Tyr166Ter
NM_001287435.1:c.351C>G	NP_001274364.1:p.Tyr117Ter
NM_004364.4:c.393C>G	NP_004355.2:p.Tyr131Ter
NM_001287424.2:c.498C>G	NP_001274353.1:p.Tyr166Ter
NM_004364.5:c.393C>G MANE Select	NP_004355.2:p.Tyr131Ter
NM_001285829.2:c.36C>G	NP_001272758.1:p.Tyr12Ter
NM_001287435.2:c.351C>G	NP_001274364.1:p.Tyr117Ter