Canonical Allele Identifier: CA346001193
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21010221-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010221T>G , CM000664.2:g.21010221T>G GRCh38
NC_000002.11:g.21233093T>G , CM000664.1:g.21233093T>G GRCh37
NC_000002.10:g.21086598T>G NCBI36
NG_011793.1:g.38853A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6647A>C MANE Select ENSP00000233242.1:p.Tyr2216Ser
ENST00000616098.4:c.6647A>C ENSP00000477990.1:p.Tyr2216Ser
NM_000384.2:c.6647A>C NP_000375.2:p.Tyr2216Ser
XM_011532809.1:c.5869+512A>C XP_011531111.1:n.5869+512A>C
NM_000384.3:c.6647A>C MANE Select NP_000375.3:p.Tyr2216Ser