Canonical Allele Identifier: CA2493476930
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010983_21010985delinsGCA , CM000664.2:g.21010983_21010985delinsGCA GRCh38
NC_000002.11:g.21233855_21233857delinsGCA , CM000664.1:g.21233855_21233857delinsGCA GRCh37
NC_000002.10:g.21087360_21087362delinsGCA NCBI36
NG_011793.1:g.38089_38091delinsTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5883_5885delinsTGC MANE Select ENSP00000233242.1:p.Ser1961=
ENST00000616098.4:c.5883_5885delinsTGC ENSP00000477990.1:p.Ser1961=
NM_000384.2:c.5883_5885delinsTGC NP_000375.2:p.Ser1961=
XM_011532809.1:c.5864+19_5864+21delinsTGC XP_011531111.1:n.5864+19_5864+21delinsTGC
NM_000384.3:c.5883_5885delinsTGC MANE Select NP_000375.3:p.Ser1961=
Search 100 bp 5'
Search 100 bp 3'