Canonical Allele Identifier: CA405275060

Gene: CEBPA

Linked Data

• dbSNP Id: rs919904139
• MyVariant Identifiers: chr19:g.33792933C>G (hg19) ; chr19:g.33302027C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33302027C>G , CM000681.2:g.33302027C>G	GRCh38
NC_000019.9:g.33792933C>G , CM000681.1:g.33792933C>G	GRCh37
NC_000019.8:g.38484773C>G	NCBI36
NG_012022.1:g.5498G>C , LRG_456:g.5498G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498907.3:c.388G>C MANE Select	ENSP00000427514.1:p.Gly130Arg
ENST00000498907.2:c.388G>C	ENSP00000427514.1:p.Gly130Arg
NM_001285829.1:c.31G>C	NP_001272758.1:p.Gly11Arg
NM_001287424.1:c.493G>C	NP_001274353.1:p.Gly165Arg
NM_001287435.1:c.346G>C	NP_001274364.1:p.Gly116Arg
NM_004364.4:c.388G>C	NP_004355.2:p.Gly130Arg
NM_001287424.2:c.493G>C	NP_001274353.1:p.Gly165Arg
NM_004364.5:c.388G>C MANE Select	NP_004355.2:p.Gly130Arg
NM_001285829.2:c.31G>C	NP_001272758.1:p.Gly11Arg
NM_001287435.2:c.346G>C	NP_001274364.1:p.Gly116Arg