Canonical Allele Identifier: CA346008827

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21238093T>G (hg19) ; chr2:g.21015221T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015221T>G , CM000664.2:g.21015221T>G	GRCh38
NC_000002.11:g.21238093T>G , CM000664.1:g.21238093T>G	GRCh37
NC_000002.10:g.21091598T>G	NCBI36
NG_011793.1:g.33853A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2854A>C	ENSP00000501110.2:n.*2854A>C
ENST00000673882.2:c.*2643A>C	ENSP00000501253.2:n.*2643A>C
ENST00000673739.1:c.3262A>C	ENSP00000501110.1:n.3262A>C
ENST00000673882.1:c.3051A>C	ENSP00000501253.1:n.3051A>C
ENST00000233242.5:c.3548A>C MANE Select	ENSP00000233242.1:p.Asn1183Thr
ENST00000616098.4:c.3548A>C	ENSP00000477990.1:p.Asn1183Thr
NM_000384.2:c.3548A>C	NP_000375.2:p.Asn1183Thr
XM_011532809.1:c.3548A>C	XP_011531111.1:p.Asn1183Thr
NM_000384.3:c.3548A>C MANE Select	NP_000375.3:p.Asn1183Thr