Canonical Allele Identifier: CA507007838
Gene: CEBPA HGNC NCBI

Linked Data

dbSNP Id: rs1967185905
MyVariant Identifiers: chr19:g.33792931G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33302025G>A , CM000681.2:g.33302025G>A GRCh38
NC_000019.9:g.33792931G>A , CM000681.1:g.33792931G>A GRCh37
NC_000019.8:g.38484771G>A NCBI36
NG_012022.1:g.5500C>T , LRG_456:g.5500C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.390C>T MANE Select ENSP00000427514.1:p.Gly130=
ENST00000498907.2:c.390C>T ENSP00000427514.1:p.Gly130=
NM_001285829.1:c.33C>T NP_001272758.1:p.Gly11=
NM_001287424.1:c.495C>T NP_001274353.1:p.Gly165=
NM_001287435.1:c.348C>T NP_001274364.1:p.Gly116=
NM_004364.4:c.390C>T NP_004355.2:p.Gly130=
NM_001287424.2:c.495C>T NP_001274353.1:p.Gly165=
NM_004364.5:c.390C>T MANE Select NP_004355.2:p.Gly130=
NM_001285829.2:c.33C>T NP_001272758.1:p.Gly11=
NM_001287435.2:c.348C>T NP_001274364.1:p.Gly116=