Canonical Allele Identifier: CA346004588
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011367T>C , CM000664.2:g.21011367T>C GRCh38
NC_000002.11:g.21234239T>C , CM000664.1:g.21234239T>C GRCh37
NC_000002.10:g.21087744T>C NCBI36
NG_011793.1:g.37707A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*4807A>G ENSP00000501110.2:n.*4807A>G
ENST00000673739.1:c.5215A>G ENSP00000501110.1:n.5215A>G
ENST00000233242.5:c.5501A>G MANE Select ENSP00000233242.1:p.Asn1834Ser
ENST00000616098.4:c.5501A>G ENSP00000477990.1:p.Asn1834Ser
NM_000384.2:c.5501A>G NP_000375.2:p.Asn1834Ser
XM_011532809.1:c.5501A>G XP_011531111.1:p.Asn1834Ser
NM_000384.3:c.5501A>G MANE Select NP_000375.3:p.Asn1834Ser