Canonical Allele Identifier: CA2493472840
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002183_21002184delinsGT , CM000664.2:g.21002183_21002184delinsGT GRCh38
NC_000002.11:g.21225055_21225056delinsGT , CM000664.1:g.21225055_21225056delinsGT GRCh37
NC_000002.10:g.21078560_21078561delinsGT NCBI36
NG_011793.1:g.46890_46891delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13238_13239delinsAC MANE Select ENSP00000233242.1:p.Asn4413=
ENST00000616098.4:c.13236_13237delinsAC ENSP00000477990.1:n.13236_13237delinsAC
NM_000384.2:c.13238_13239delinsAC NP_000375.2:p.Asn4413=
XM_011532809.1:c.5870-2911_5870-2910delinsAC XP_011531111.1:n.5870-2911_5870-2910delinsAC
NM_000384.3:c.13238_13239delinsAC MANE Select NP_000375.3:p.Asn4413=