Canonical Allele Identifier: CA531312791

Gene: APOB

Linked Data

• dbSNP Id: rs1207192709
• gnomAD v2: 2-21238166-C-A
• gnomAD v4: 2-21015294-C-A
• MyVariant Identifiers: chr2:g.21238166C>A (hg19) ; chr2:g.21015294C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015294C>A , CM000664.2:g.21015294C>A	GRCh38
NC_000002.11:g.21238166C>A , CM000664.1:g.21238166C>A	GRCh37
NC_000002.10:g.21091671C>A	NCBI36
NG_011793.1:g.33780G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2815-34G>T	ENSP00000501110.2:n.*2815-34G>T
ENST00000673882.2:c.*2604-34G>T	ENSP00000501253.2:n.*2604-34G>T
ENST00000673739.1:c.3223-34G>T	ENSP00000501110.1:n.3223-34G>T
ENST00000673882.1:c.3012-34G>T	ENSP00000501253.1:n.3012-34G>T
ENST00000233242.5:c.3509-34G>T MANE Select	ENSP00000233242.1:n.3509-34G>T
ENST00000616098.4:c.3509-34G>T	ENSP00000477990.1:n.3509-34G>T
NM_000384.2:c.3509-34G>T	NP_000375.2:n.3509-34G>T
XM_011532809.1:c.3509-34G>T	XP_011531111.1:n.3509-34G>T
NM_000384.3:c.3509-34G>T MANE Select	NP_000375.3:n.3509-34G>T