Canonical Allele Identifier: CA346004654
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011397G>A , CM000664.2:g.21011397G>A GRCh38
NC_000002.11:g.21234269G>A , CM000664.1:g.21234269G>A GRCh37
NC_000002.10:g.21087774G>A NCBI36
NG_011793.1:g.37677C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*4777C>T ENSP00000501110.2:n.*4777C>T
ENST00000673739.1:c.5185C>T ENSP00000501110.1:n.5185C>T
ENST00000233242.5:c.5471C>T MANE Select ENSP00000233242.1:p.Ala1824Val
ENST00000616098.4:c.5471C>T ENSP00000477990.1:p.Ala1824Val
NM_000384.2:c.5471C>T NP_000375.2:p.Ala1824Val
XM_011532809.1:c.5471C>T XP_011531111.1:p.Ala1824Val
NM_000384.3:c.5471C>T MANE Select NP_000375.3:p.Ala1824Val