Canonical Allele Identifier: CA2698847680

Gene: APOB

Linked Data

• dbSNP Id: rs2103370422

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21023198T>G , CM000664.2:g.21023198T>G	GRCh38
NC_000002.11:g.21246070T>G , CM000664.1:g.21246070T>G	GRCh37
NC_000002.10:g.21099575T>G	NCBI36
NG_011793.1:g.25876A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*1911-156A>C	ENSP00000501110.2:n.*1911-156A>C
ENST00000673882.2:c.*1911-156A>C	ENSP00000501253.2:n.*1911-156A>C
ENST00000673739.1:c.2319-156A>C	ENSP00000501110.1:n.2319-156A>C
ENST00000673882.1:c.2319-156A>C	ENSP00000501253.1:n.2319-156A>C
ENST00000233242.5:c.2605-156A>C MANE Select	ENSP00000233242.1:n.2605-156A>C
ENST00000616098.4:c.2605-156A>C	ENSP00000477990.1:n.2605-156A>C
NM_000384.2:c.2605-156A>C	NP_000375.2:n.2605-156A>C
XM_011532809.1:c.2605-156A>C	XP_011531111.1:n.2605-156A>C
NM_000384.3:c.2605-156A>C MANE Select	NP_000375.3:n.2605-156A>C