Canonical Allele Identifier: CA307843807
Gene: CEBPA HGNC NCBI

Linked Data

dbSNP Id: rs976861369
gnomAD v3: 19-33300472-T-TA
gnomAD v4: 19-33300472-T-TA
MyVariant Identifiers: chr19:g.33791378_33791379insA (hg19) chr19:g.33300472_33300473insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33300473dup , CM000681.2:g.33300473dup GRCh38
NC_000019.9:g.33791379dup , CM000681.1:g.33791379dup GRCh37
NC_000019.8:g.38483219dup NCBI36
NG_012022.1:g.7052dup , LRG_456:g.7052dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.*865dup MANE Select ENSP00000427514.1:n.*865dup
ENST00000498907.2:c.*865dup ENSP00000427514.1:n.*865dup
NM_001285829.1:c.*865dup NP_001272758.1:n.*865dup
NM_001287424.1:c.*865dup NP_001274353.1:n.*865dup
NM_001287435.1:c.*865dup NP_001274364.1:n.*865dup
NM_004364.4:c.*865dup NP_004355.2:n.*865dup
NM_001287424.2:c.*865dup NP_001274353.1:n.*865dup
NM_004364.5:c.*865dup MANE Select NP_004355.2:n.*865dup
NM_001285829.2:c.*865dup NP_001272758.1:n.*865dup
NM_001287435.2:c.*865dup NP_001274364.1:n.*865dup
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