Canonical Allele Identifier: CA345977607
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1216474211
gnomAD v2: 2-21228029-T-A
MyVariant Identifiers: chr2:g.21228029T>A (hg19) chr2:g.21005157T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21005157T>A , CM000664.2:g.21005157T>A GRCh38
NC_000002.11:g.21228029T>A , CM000664.1:g.21228029T>A GRCh37
NC_000002.10:g.21081534T>A NCBI36
NG_011793.1:g.43917A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.11711A>T MANE Select ENSP00000233242.1:p.Asn3904Ile
ENST00000616098.4:c.11711A>T ENSP00000477990.1:p.Asn3904Ile
NM_000384.2:c.11711A>T NP_000375.2:p.Asn3904Ile
XM_011532809.1:c.5869+5576A>T XP_011531111.1:n.5869+5576A>T
NM_000384.3:c.11711A>T MANE Select NP_000375.3:p.Asn3904Ile
Search 100 bp 5'
Search 100 bp 3'