Canonical Allele Identifier: CA2698843600

Gene: APOB

Linked Data

• dbSNP Id: rs2103362323

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21014910T>G , CM000664.2:g.21014910T>G	GRCh38
NC_000002.11:g.21237782T>G , CM000664.1:g.21237782T>G	GRCh37
NC_000002.10:g.21091287T>G	NCBI36
NG_011793.1:g.34164A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*3002+163A>C	ENSP00000501110.2:n.*3002+163A>C
ENST00000673882.2:c.*2791+163A>C	ENSP00000501253.2:n.*2791+163A>C
ENST00000673739.1:c.3410+163A>C	ENSP00000501110.1:n.3410+163A>C
ENST00000673882.1:c.3199+163A>C	ENSP00000501253.1:n.3199+163A>C
ENST00000233242.5:c.3696+163A>C MANE Select	ENSP00000233242.1:n.3696+163A>C
ENST00000616098.4:c.3696+163A>C	ENSP00000477990.1:n.3696+163A>C
NM_000384.2:c.3696+163A>C	NP_000375.2:n.3696+163A>C
XM_011532809.1:c.3696+163A>C	XP_011531111.1:n.3696+163A>C
NM_000384.3:c.3696+163A>C MANE Select	NP_000375.3:n.3696+163A>C