Canonical Allele Identifier: CA346003838
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21011016-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011016C>T , CM000664.2:g.21011016C>T GRCh38
NC_000002.11:g.21233888C>T , CM000664.1:g.21233888C>T GRCh37
NC_000002.10:g.21087393C>T NCBI36
NG_011793.1:g.38058G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5852G>A MANE Select ENSP00000233242.1:p.Ser1951Asn
ENST00000616098.4:c.5852G>A ENSP00000477990.1:p.Ser1951Asn
NM_000384.2:c.5852G>A NP_000375.2:p.Ser1951Asn
XM_011532809.1:c.5852G>A XP_011531111.1:p.Ser1951Asn
NM_000384.3:c.5852G>A MANE Select NP_000375.3:p.Ser1951Asn