Canonical Allele Identifier: CA764121124

Gene: APOB

Linked Data

• dbSNP Id: rs1457685136
• gnomAD v3: 2-21021093-A-G
• gnomAD v4: 2-21021093-A-G
• MyVariant Identifiers: chr2:g.21243965A>G (hg19) ; chr2:g.21021093A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21021093A>G , CM000664.2:g.21021093A>G	GRCh38
NC_000002.11:g.21243965A>G , CM000664.1:g.21243965A>G	GRCh37
NC_000002.10:g.21097470A>G	NCBI36
NG_011793.1:g.27981T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2123-1188T>C	ENSP00000501110.2:n.*2123-1188T>C
ENST00000673882.2:c.*2123-1188T>C	ENSP00000501253.2:n.*2123-1188T>C
ENST00000673739.1:c.2531-1188T>C	ENSP00000501110.1:n.2531-1188T>C
ENST00000673882.1:c.2531-1188T>C	ENSP00000501253.1:n.2531-1188T>C
ENST00000233242.5:c.2817-1188T>C MANE Select	ENSP00000233242.1:n.2817-1188T>C
ENST00000616098.4:c.2817-1188T>C	ENSP00000477990.1:n.2817-1188T>C
NM_000384.2:c.2817-1188T>C	NP_000375.2:n.2817-1188T>C
XM_011532809.1:c.2817-1188T>C	XP_011531111.1:n.2817-1188T>C
NM_000384.3:c.2817-1188T>C MANE Select	NP_000375.3:n.2817-1188T>C