Canonical Allele Identifier: CA2658056870
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21015041-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21015041A>G , CM000664.2:g.21015041A>G GRCh38
NC_000002.11:g.21237913A>G , CM000664.1:g.21237913A>G GRCh37
NC_000002.10:g.21091418A>G NCBI36
NG_011793.1:g.34033T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*3002+32T>C ENSP00000501110.2:n.*3002+32T>C
ENST00000673882.2:c.*2791+32T>C ENSP00000501253.2:n.*2791+32T>C
ENST00000673739.1:c.3410+32T>C ENSP00000501110.1:n.3410+32T>C
ENST00000673882.1:c.3199+32T>C ENSP00000501253.1:n.3199+32T>C
ENST00000233242.5:c.3696+32T>C MANE Select ENSP00000233242.1:n.3696+32T>C
ENST00000616098.4:c.3696+32T>C ENSP00000477990.1:n.3696+32T>C
NM_000384.2:c.3696+32T>C NP_000375.2:n.3696+32T>C
XM_011532809.1:c.3696+32T>C XP_011531111.1:n.3696+32T>C
NM_000384.3:c.3696+32T>C MANE Select NP_000375.3:n.3696+32T>C
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