Canonical Allele Identifier: CA425346267

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21234232T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21011360T>G , CM000664.2:g.21011360T>G	GRCh38
NC_000002.11:g.21234232T>G , CM000664.1:g.21234232T>G	GRCh37
NC_000002.10:g.21087737T>G	NCBI36
NG_011793.1:g.37714A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*4814A>C	ENSP00000501110.2:n.*4814A>C
ENST00000673739.1:c.5222A>C	ENSP00000501110.1:n.5222A>C
ENST00000233242.5:c.5508A>C MANE Select	ENSP00000233242.1:p.Ile1836=
ENST00000616098.4:c.5508A>C	ENSP00000477990.1:p.Ile1836=
NM_000384.2:c.5508A>C	NP_000375.2:p.Ile1836=
XM_011532809.1:c.5508A>C	XP_011531111.1:p.Ile1836=
NM_000384.3:c.5508A>C MANE Select	NP_000375.3:p.Ile1836=