Canonical Allele Identifier: CA2576686786
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs2103370679
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21023454A>G , CM000664.2:g.21023454A>G GRCh38
NC_000002.11:g.21246326A>G , CM000664.1:g.21246326A>G GRCh37
NC_000002.10:g.21099831A>G NCBI36
NG_011793.1:g.25620T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*1910+71T>C ENSP00000501110.2:n.*1910+71T>C
ENST00000673882.2:c.*1910+71T>C ENSP00000501253.2:n.*1910+71T>C
ENST00000673739.1:c.2318+71T>C ENSP00000501110.1:n.2318+71T>C
ENST00000673882.1:c.2318+71T>C ENSP00000501253.1:n.2318+71T>C
ENST00000233242.5:c.2604+71T>C MANE Select ENSP00000233242.1:n.2604+71T>C
ENST00000616098.4:c.2604+71T>C ENSP00000477990.1:n.2604+71T>C
NM_000384.2:c.2604+71T>C NP_000375.2:n.2604+71T>C
XM_011532809.1:c.2604+71T>C XP_011531111.1:n.2604+71T>C
NM_000384.3:c.2604+71T>C MANE Select NP_000375.3:n.2604+71T>C
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