Canonical Allele Identifier: CA2493476657
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010339A= , CM000664.2:g.21010339A= GRCh38
NC_000002.11:g.21233211A= , CM000664.1:g.21233211A= GRCh37
NC_000002.10:g.21086716A= NCBI36
NG_011793.1:g.38735T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6529T= MANE Select ENSP00000233242.1:p.Tyr2177=
ENST00000616098.4:c.6529T= ENSP00000477990.1:p.Tyr2177=
NM_000384.2:c.6529T= NP_000375.2:p.Tyr2177=
XM_011532809.1:c.5869+394T= XP_011531111.1:n.5869+394T=
NM_000384.3:c.6529T= MANE Select NP_000375.3:p.Tyr2177=