Canonical Allele Identifier: CA346003818
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011008G>T , CM000664.2:g.21011008G>T GRCh38
NC_000002.11:g.21233880G>T , CM000664.1:g.21233880G>T GRCh37
NC_000002.10:g.21087385G>T NCBI36
NG_011793.1:g.38066C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5860C>A MANE Select ENSP00000233242.1:p.Leu1954Ile
ENST00000616098.4:c.5860C>A ENSP00000477990.1:p.Leu1954Ile
NM_000384.2:c.5860C>A NP_000375.2:p.Leu1954Ile
XM_011532809.1:c.5860C>A XP_011531111.1:p.Leu1954Ile
NM_000384.3:c.5860C>A MANE Select NP_000375.3:p.Leu1954Ile