Canonical Allele Identifier: CA345968502
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21225093A>C (hg19) chr2:g.21002221A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002221A>C , CM000664.2:g.21002221A>C GRCh38
NC_000002.11:g.21225093A>C , CM000664.1:g.21225093A>C GRCh37
NC_000002.10:g.21078598A>C NCBI36
NG_011793.1:g.46853T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13201T>G MANE Select ENSP00000233242.1:p.Tyr4401Asp
ENST00000616098.4:c.13199T>G ENSP00000477990.1:n.13199T>G
NM_000384.2:c.13201T>G NP_000375.2:p.Tyr4401Asp
XM_011532809.1:c.5870-2948T>G XP_011531111.1:n.5870-2948T>G
NM_000384.3:c.13201T>G MANE Select NP_000375.3:p.Tyr4401Asp
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