Canonical Allele Identifier: CA345977151
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1047501521
gnomAD v4: 2-21005081-A-T
MyVariant Identifiers: chr2:g.21227953A>T (hg19) chr2:g.21005081A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21005081A>T , CM000664.2:g.21005081A>T GRCh38
NC_000002.11:g.21227953A>T , CM000664.1:g.21227953A>T GRCh37
NC_000002.10:g.21081458A>T NCBI36
NG_011793.1:g.43993T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.11787T>A MANE Select ENSP00000233242.1:p.Asn3929Lys
ENST00000616098.4:c.11787T>A ENSP00000477990.1:p.Asn3929Lys
NM_000384.2:c.11787T>A NP_000375.2:p.Asn3929Lys
XM_011532809.1:c.5869+5652T>A XP_011531111.1:n.5869+5652T>A
NM_000384.3:c.11787T>A MANE Select NP_000375.3:p.Asn3929Lys
Search 100 bp 5'
Search 100 bp 3'