Canonical Allele Identifier: CA2493476987
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011075G= , CM000664.2:g.21011075G= GRCh38
NC_000002.11:g.21233947G= , CM000664.1:g.21233947G= GRCh37
NC_000002.10:g.21087452G= NCBI36
NG_011793.1:g.37999C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5793C= MANE Select ENSP00000233242.1:p.Phe1931=
ENST00000616098.4:c.5793C= ENSP00000477990.1:p.Phe1931=
NM_000384.2:c.5793C= NP_000375.2:p.Phe1931=
XM_011532809.1:c.5793C= XP_011531111.1:p.Phe1931=
NM_000384.3:c.5793C= MANE Select NP_000375.3:p.Phe1931=
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