Canonical Allele Identifier: CA1028215580
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs571938001
gnomAD v3: 2-21021140-A-C
gnomAD v4: 2-21021140-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21021140A>C , CM000664.2:g.21021140A>C GRCh38
NC_000002.11:g.21244012A>C , CM000664.1:g.21244012A>C GRCh37
NC_000002.10:g.21097517A>C NCBI36
NG_011793.1:g.27934T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.2:c.*2123-1235T>G ENSP00000501110.2:n.*2123-1235T>G
ENST00000673882.2:c.*2123-1235T>G ENSP00000501253.2:n.*2123-1235T>G
ENST00000673739.1:c.2531-1235T>G ENSP00000501110.1:n.2531-1235T>G
ENST00000673882.1:c.2531-1235T>G ENSP00000501253.1:n.2531-1235T>G
ENST00000233242.5:c.2817-1235T>G MANE Select ENSP00000233242.1:n.2817-1235T>G
ENST00000616098.4:c.2817-1235T>G ENSP00000477990.1:n.2817-1235T>G
NM_000384.2:c.2817-1235T>G NP_000375.2:n.2817-1235T>G
XM_011532809.1:c.2817-1235T>G XP_011531111.1:n.2817-1235T>G
NM_000384.3:c.2817-1235T>G MANE Select NP_000375.3:n.2817-1235T>G