Canonical Allele Identifier: CA345970263
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21225402T>A (hg19) chr2:g.21002530T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002530T>A , CM000664.2:g.21002530T>A GRCh38
NC_000002.11:g.21225402T>A , CM000664.1:g.21225402T>A GRCh37
NC_000002.10:g.21078907T>A NCBI36
NG_011793.1:g.46544A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.12892A>T MANE Select ENSP00000233242.1:p.Asn4298Tyr
ENST00000616098.4:c.12892A>T ENSP00000477990.1:p.Asn4298Tyr
NM_000384.2:c.12892A>T NP_000375.2:p.Asn4298Tyr
XM_011532809.1:c.5870-3257A>T XP_011531111.1:n.5870-3257A>T
NM_000384.3:c.12892A>T MANE Select NP_000375.3:p.Asn4298Tyr
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