Canonical Allele Identifier: CA916488027

Gene: APOB

Linked Data

• dbSNP Id: rs1572783990

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21011006_21011007insGG , CM000664.2:g.21011006_21011007insGG	GRCh38
NC_000002.11:g.21233878_21233879insGG , CM000664.1:g.21233878_21233879insGG	GRCh37
NC_000002.10:g.21087383_21087384insGG	NCBI36
NG_011793.1:g.38068_38069insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.5862_5863insCC MANE Select	ENSP00000233242.1:p.Val1955ProfsTer?
ENST00000616098.4:c.5862_5863insCC	ENSP00000477990.1:p.Val1955ProfsTer?
NM_000384.2:c.5862_5863insCC	NP_000375.2:p.Val1955ProfsTer?
XM_011532809.1:c.5862_5863insCC	XP_011531111.1:p.Val1955ProfsTer?
NM_000384.3:c.5862_5863insCC MANE Select	NP_000375.3:p.Val1955ProfsTer?