Canonical Allele Identifier: CA346008847

Gene: APOB

Linked Data

• gnomAD v4: 2-21015231-T-C
• MyVariant Identifiers: chr2:g.21238103T>C (hg19) ; chr2:g.21015231T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015231T>C , CM000664.2:g.21015231T>C	GRCh38
NC_000002.11:g.21238103T>C , CM000664.1:g.21238103T>C	GRCh37
NC_000002.10:g.21091608T>C	NCBI36
NG_011793.1:g.33843A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2844A>G	ENSP00000501110.2:n.*2844A>G
ENST00000673882.2:c.*2633A>G	ENSP00000501253.2:n.*2633A>G
ENST00000673739.1:c.3252A>G	ENSP00000501110.1:n.3252A>G
ENST00000673882.1:c.3041A>G	ENSP00000501253.1:n.3041A>G
ENST00000233242.5:c.3538A>G MANE Select	ENSP00000233242.1:p.Thr1180Ala
ENST00000616098.4:c.3538A>G	ENSP00000477990.1:p.Thr1180Ala
NM_000384.2:c.3538A>G	NP_000375.2:p.Thr1180Ala
XM_011532809.1:c.3538A>G	XP_011531111.1:p.Thr1180Ala
NM_000384.3:c.3538A>G MANE Select	NP_000375.3:p.Thr1180Ala