Canonical Allele Identifier: CA052042
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs771015234
ExAC: 2:21225126 C / A
gnomAD v2: 2-21225126-C-A
gnomAD v4: 2-21002254-C-A
MyVariant Identifiers: chr2:g.21225126C>A (hg19) chr2:g.21002254C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002254C>A , CM000664.2:g.21002254C>A GRCh38
NC_000002.11:g.21225126C>A , CM000664.1:g.21225126C>A GRCh37
NC_000002.10:g.21078631C>A NCBI36
NG_011793.1:g.46820G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13168G>T MANE Select ENSP00000233242.1:p.Asp4390Tyr
ENST00000616098.4:c.13166G>T ENSP00000477990.1:n.13166G>T
NM_000384.2:c.13168G>T NP_000375.2:p.Asp4390Tyr
XM_011532809.1:c.5870-2981G>T XP_011531111.1:n.5870-2981G>T
NM_000384.3:c.13168G>T MANE Select NP_000375.3:p.Asp4390Tyr
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