Canonical Allele Identifier: CA507007751

Gene: CEBPA

Linked Data

• gnomAD v4: 19-33301920-G-A
• MyVariant Identifiers: chr19:g.33792826G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33301920G>A , CM000681.2:g.33301920G>A	GRCh38
NC_000019.9:g.33792826G>A , CM000681.1:g.33792826G>A	GRCh37
NC_000019.8:g.38484666G>A	NCBI36
NG_012022.1:g.5605C>T , LRG_456:g.5605C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000498907.3:c.495C>T MANE Select	ENSP00000427514.1:p.Arg165=
ENST00000498907.2:c.495C>T	ENSP00000427514.1:p.Arg165=
NM_001285829.1:c.138C>T	NP_001272758.1:p.Arg46=
NM_001287424.1:c.600C>T	NP_001274353.1:p.Arg200=
NM_001287435.1:c.453C>T	NP_001274364.1:p.Arg151=
NM_004364.4:c.495C>T	NP_004355.2:p.Arg165=
NM_001287424.2:c.600C>T	NP_001274353.1:p.Arg200=
NM_004364.5:c.495C>T MANE Select	NP_004355.2:p.Arg165=
NM_001285829.2:c.138C>T	NP_001272758.1:p.Arg46=
NM_001287435.2:c.453C>T	NP_001274364.1:p.Arg151=