Canonical Allele Identifier: CA052138
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs750727165
gnomAD v2: 2-21225092-T-C
gnomAD v4: 2-21002220-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002220T>C , CM000664.2:g.21002220T>C GRCh38
NC_000002.11:g.21225092T>C , CM000664.1:g.21225092T>C GRCh37
NC_000002.10:g.21078597T>C NCBI36
NG_011793.1:g.46854A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13202A>G MANE Select ENSP00000233242.1:p.Tyr4401Cys
ENST00000616098.4:c.13200A>G ENSP00000477990.1:n.13200A>G
NM_000384.2:c.13202A>G NP_000375.2:p.Tyr4401Cys
XM_011532809.1:c.5870-2947A>G XP_011531111.1:n.5870-2947A>G
NM_000384.3:c.13202A>G MANE Select NP_000375.3:p.Tyr4401Cys