Canonical Allele Identifier: CA2493476258
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009488_21009489delinsTG , CM000664.2:g.21009488_21009489delinsTG GRCh38
NC_000002.11:g.21232360_21232361delinsTG , CM000664.1:g.21232360_21232361delinsTG GRCh37
NC_000002.10:g.21085865_21085866delinsTG NCBI36
NG_011793.1:g.39585_39586delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.7379_7380delinsCA MANE Select ENSP00000233242.1:p.Pro2460=
ENST00000616098.4:c.7379_7380delinsCA ENSP00000477990.1:p.Pro2460=
NM_000384.2:c.7379_7380delinsCA NP_000375.2:p.Pro2460=
XM_011532809.1:c.5869+1244_5869+1245delinsCA XP_011531111.1:n.5869+1244_5869+1245delinsCA
NM_000384.3:c.7379_7380delinsCA MANE Select NP_000375.3:p.Pro2460=
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