Canonical Allele Identifier: CA425344144
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1275715955
gnomAD v2: 2-21230068-A-G
gnomAD v3: 2-21007196-A-G
gnomAD v4: 2-21007196-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007196A>G , CM000664.2:g.21007196A>G GRCh38
NC_000002.11:g.21230068A>G , CM000664.1:g.21230068A>G GRCh37
NC_000002.10:g.21083573A>G NCBI36
NG_011793.1:g.41878T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9672T>C MANE Select ENSP00000233242.1:p.Asn3224=
ENST00000616098.4:c.9672T>C ENSP00000477990.1:p.Asn3224=
NM_000384.2:c.9672T>C NP_000375.2:p.Asn3224=
XM_011532809.1:c.5869+3537T>C XP_011531111.1:n.5869+3537T>C
NM_000384.3:c.9672T>C MANE Select NP_000375.3:p.Asn3224=