Canonical Allele Identifier: CA507007616

Gene: CEBPA

Linked Data

• gnomAD v4: 19-33302253-G-T
• MyVariant Identifiers: chr19:g.33793159G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33302253G>T , CM000681.2:g.33302253G>T	GRCh38
NC_000019.9:g.33793159G>T , CM000681.1:g.33793159G>T	GRCh37
NC_000019.8:g.38484999G>T	NCBI36
NG_012022.1:g.5272C>A , LRG_456:g.5272C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.162C>A MANE Select	ENSP00000427514.1:p.Gly54=
ENST00000498907.2:c.162C>A	ENSP00000427514.1:p.Gly54=
NM_001285829.1:c.-196C>A	NP_001272758.1:n.-196C>A
NM_001287424.1:c.267C>A	NP_001274353.1:p.Gly89=
NM_001287435.1:c.120C>A	NP_001274364.1:p.Gly40=
NM_004364.4:c.162C>A	NP_004355.2:p.Gly54=
NM_001287424.2:c.267C>A	NP_001274353.1:p.Gly89=
NM_004364.5:c.162C>A MANE Select	NP_004355.2:p.Gly54=
NM_001285829.2:c.-196C>A	NP_001272758.1:n.-196C>A
NM_001287435.2:c.120C>A	NP_001274364.1:p.Gly40=