Canonical Allele Identifier: CA43513572

Gene: APOB

Linked Data

• dbSNP Id: rs141422999
• MyVariant Identifiers: chr2:g.21237944C>G (hg19) ; chr2:g.21015072C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015072C>G , CM000664.2:g.21015072C>G	GRCh38
NC_000002.11:g.21237944C>G , CM000664.1:g.21237944C>G	GRCh37
NC_000002.10:g.21091449C>G	NCBI36
NG_011793.1:g.34002G>C

Transcript Alleles

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