Canonical Allele Identifier: CA531312773

Gene: APOB

Linked Data

• dbSNP Id: rs1234097185
• gnomAD v2: 2-21237800-A-AC
• gnomAD v3: 2-21014928-A-AC
• gnomAD v4: 2-21014928-A-AC
• MyVariant Identifiers: chr2:g.21237800_21237801insC (hg19) ; chr2:g.21014928_21014929insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21014928_21014929insC , CM000664.2:g.21014928_21014929insC	GRCh38
NC_000002.11:g.21237800_21237801insC , CM000664.1:g.21237800_21237801insC	GRCh37
NC_000002.10:g.21091305_21091306insC	NCBI36
NG_011793.1:g.34145_34146insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*3002+144_*3002+145insG	ENSP00000501110.2:n.*3002+144_*3002+145insG
ENST00000673882.2:c.*2791+144_*2791+145insG	ENSP00000501253.2:n.*2791+144_*2791+145insG
ENST00000673739.1:c.3410+144_3410+145insG	ENSP00000501110.1:n.3410+144_3410+145insG
ENST00000673882.1:c.3199+144_3199+145insG	ENSP00000501253.1:n.3199+144_3199+145insG
ENST00000233242.5:c.3696+144_3696+145insG MANE Select	ENSP00000233242.1:n.3696+144_3696+145insG
ENST00000616098.4:c.3696+144_3696+145insG	ENSP00000477990.1:n.3696+144_3696+145insG
NM_000384.2:c.3696+144_3696+145insG	NP_000375.2:n.3696+144_3696+145insG
XM_011532809.1:c.3696+144_3696+145insG	XP_011531111.1:n.3696+144_3696+145insG
NM_000384.3:c.3696+144_3696+145insG MANE Select	NP_000375.3:n.3696+144_3696+145insG