Canonical Allele Identifier: CA633070015
Gene: CEBPA HGNC NCBI

Linked Data

dbSNP Id: rs1225577002
gnomAD v2: 19-33791333-A-AT
gnomAD v3: 19-33300427-A-AT
gnomAD v4: 19-33300427-A-AT
MyVariant Identifiers: chr19:g.33791333_33791334insT (hg19) chr19:g.33300427_33300428insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33300428dup , CM000681.2:g.33300428dup GRCh38
NC_000019.9:g.33791334dup , CM000681.1:g.33791334dup GRCh37
NC_000019.8:g.38483174dup NCBI36
NG_012022.1:g.7097dup , LRG_456:g.7097dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000498907.3:c.*910dup MANE Select ENSP00000427514.1:n.*910dup
ENST00000498907.2:c.*910dup ENSP00000427514.1:n.*910dup
NM_001285829.1:c.*910dup NP_001272758.1:n.*910dup
NM_001287424.1:c.*910dup NP_001274353.1:n.*910dup
NM_001287435.1:c.*910dup NP_001274364.1:n.*910dup
NM_004364.4:c.*910dup NP_004355.2:n.*910dup
NM_001287424.2:c.*910dup NP_001274353.1:n.*910dup
NM_004364.5:c.*910dup MANE Select NP_004355.2:n.*910dup
NM_001285829.2:c.*910dup NP_001272758.1:n.*910dup
NM_001287435.2:c.*910dup NP_001274364.1:n.*910dup
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Search 100 bp 3'