Canonical Allele Identifier: CA346009101

Gene: APOB

Linked Data

• gnomAD v4: 2-21015448-C-A
• MyVariant Identifiers: chr2:g.21238320C>A (hg19) ; chr2:g.21015448C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015448C>A , CM000664.2:g.21015448C>A	GRCh38
NC_000002.11:g.21238320C>A , CM000664.1:g.21238320C>A	GRCh37
NC_000002.10:g.21091825C>A	NCBI36
NG_011793.1:g.33626G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2736G>T	ENSP00000501110.2:n.*2736G>T
ENST00000673882.2:c.*2525G>T	ENSP00000501253.2:n.*2525G>T
ENST00000673739.1:c.3144G>T	ENSP00000501110.1:n.3144G>T
ENST00000673882.1:c.2933G>T	ENSP00000501253.1:n.2933G>T
ENST00000233242.5:c.3430G>T MANE Select	ENSP00000233242.1:p.Ala1144Ser
ENST00000616098.4:c.3430G>T	ENSP00000477990.1:p.Ala1144Ser
NM_000384.2:c.3430G>T	NP_000375.2:p.Ala1144Ser
XM_011532809.1:c.3430G>T	XP_011531111.1:p.Ala1144Ser
NM_000384.3:c.3430G>T MANE Select	NP_000375.3:p.Ala1144Ser