Canonical Allele Identifier: CA2493488739
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs520354
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21036740A>T , CM000664.2:g.21036740A>T GRCh38
NC_000002.11:g.21259612A>T , CM000664.1:g.21259612A>T GRCh37
NC_000002.10:g.21113117A>T NCBI36
NG_011793.1:g.12334T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.2:c.539+360T>A ENSP00000501110.2:n.539+360T>A
ENST00000673882.2:c.539+360T>A ENSP00000501253.2:n.539+360T>A
ENST00000673739.1:c.407+360T>A ENSP00000501110.1:n.407+360T>A
ENST00000673882.1:c.407+360T>A ENSP00000501253.1:n.407+360T>A
ENST00000233242.5:c.693+360T>A MANE Select ENSP00000233242.1:n.693+360T>A
ENST00000399256.4:c.693+360T>A ENSP00000382200.4:n.693+360T>A
ENST00000616098.4:c.693+360T>A ENSP00000477990.1:n.693+360T>A
NM_000384.2:c.693+360T>A NP_000375.2:n.693+360T>A
XM_011532809.1:c.693+360T>A XP_011531111.1:n.693+360T>A
NM_000384.3:c.693+360T>A MANE Select NP_000375.3:n.693+360T>A
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