Canonical Allele Identifier: CA425120945

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21260838A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21037966A>G , CM000664.2:g.21037966A>G	GRCh38
NC_000002.11:g.21260838A>G , CM000664.1:g.21260838A>G	GRCh37
NC_000002.10:g.21114343A>G	NCBI36
NG_011793.1:g.11108T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.384-711T>C	ENSP00000501110.2:n.384-711T>C
ENST00000673882.2:c.384-711T>C	ENSP00000501253.2:n.384-711T>C
ENST00000673739.1:c.252-711T>C	ENSP00000501110.1:n.252-711T>C
ENST00000673882.1:c.252-711T>C	ENSP00000501253.1:n.252-711T>C
ENST00000233242.5:c.529T>C MANE Select	ENSP00000233242.1:p.Leu177=
ENST00000399256.4:c.529T>C	ENSP00000382200.4:p.Leu177=
ENST00000616098.4:c.529T>C	ENSP00000477990.1:p.Leu177=
NM_000384.2:c.529T>C	NP_000375.2:p.Leu177=
XM_011532809.1:c.529T>C	XP_011531111.1:p.Leu177=
NM_000384.3:c.529T>C MANE Select	NP_000375.3:p.Leu177=