Canonical Allele Identifier: CA345988546
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21007027-G-A
MyVariant Identifiers: chr2:g.21229899G>A (hg19) chr2:g.21007027G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007027G>A , CM000664.2:g.21007027G>A GRCh38
NC_000002.11:g.21229899G>A , CM000664.1:g.21229899G>A GRCh37
NC_000002.10:g.21083404G>A NCBI36
NG_011793.1:g.42047C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9841C>T MANE Select ENSP00000233242.1:p.Pro3281Ser
ENST00000616098.4:c.9841C>T ENSP00000477990.1:p.Pro3281Ser
NM_000384.2:c.9841C>T NP_000375.2:p.Pro3281Ser
XM_011532809.1:c.5869+3706C>T XP_011531111.1:n.5869+3706C>T
NM_000384.3:c.9841C>T MANE Select NP_000375.3:p.Pro3281Ser
Search 100 bp 5'
Search 100 bp 3'