Canonical Allele Identifier: CA764121109
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1335390161
MyVariant Identifiers: chr2:g.21243955del (hg19) chr2:g.21021083del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21021084del , CM000664.2:g.21021084del GRCh38
NC_000002.11:g.21243956del , CM000664.1:g.21243956del GRCh37
NC_000002.10:g.21097461del NCBI36
NG_011793.1:g.27991del

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*2123-1178del ENSP00000501110.2:n.*2123-1178del
ENST00000673882.2:c.*2123-1178del ENSP00000501253.2:n.*2123-1178del
ENST00000673739.1:c.2531-1178del ENSP00000501110.1:n.2531-1178del
ENST00000673882.1:c.2531-1178del ENSP00000501253.1:n.2531-1178del
ENST00000233242.5:c.2817-1178del MANE Select ENSP00000233242.1:n.2817-1178del
ENST00000616098.4:c.2817-1178del ENSP00000477990.1:n.2817-1178del
NM_000384.2:c.2817-1178del NP_000375.2:n.2817-1178del
XM_011532809.1:c.2817-1178del XP_011531111.1:n.2817-1178del
NM_000384.3:c.2817-1178del MANE Select NP_000375.3:n.2817-1178del
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