Canonical Allele Identifier: CA2493472828
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1662999649

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002172_21002173del , CM000664.2:g.21002172_21002173del GRCh38
NC_000002.11:g.21225044_21225045del , CM000664.1:g.21225044_21225045del GRCh37
NC_000002.10:g.21078549_21078550del NCBI36
NG_011793.1:g.46901_46902del

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.13249_13250del MANE Select ENSP00000233242.1:p.Ala4417SerfsTer2
ENST00000616098.4:c.13247_13248del ENSP00000477990.1:n.13247_13248del
NM_000384.2:c.13249_13250del NP_000375.2:p.Ala4417SerfsTer2
XM_011532809.1:c.5870-2900_5870-2899del XP_011531111.1:n.5870-2900_5870-2899del
NM_000384.3:c.13249_13250del MANE Select NP_000375.3:p.Ala4417SerfsTer2