Canonical Allele Identifier: CA052374
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs374044926
ExAC: 2:21224987 A / T
gnomAD v2: 2-21224987-A-T
gnomAD v3: 2-21002115-A-T
gnomAD v4: 2-21002115-A-T
MyVariant Identifiers: chr2:g.21224987A>T (hg19) chr2:g.21002115A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002115A>T , CM000664.2:g.21002115A>T GRCh38
NC_000002.11:g.21224987A>T , CM000664.1:g.21224987A>T GRCh37
NC_000002.10:g.21078492A>T NCBI36
NG_011793.1:g.46959T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13307T>A MANE Select ENSP00000233242.1:p.Leu4436His
ENST00000616098.4:c.13305T>A ENSP00000477990.1:n.13305T>A
NM_000384.2:c.13307T>A NP_000375.2:p.Leu4436His
XM_011532809.1:c.5870-2842T>A XP_011531111.1:n.5870-2842T>A
NM_000384.3:c.13307T>A MANE Select NP_000375.3:p.Leu4436His
Search 100 bp 5'
Search 100 bp 3'