Canonical Allele Identifier: CA346003826
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21011011-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011011G>C , CM000664.2:g.21011011G>C GRCh38
NC_000002.11:g.21233883G>C , CM000664.1:g.21233883G>C GRCh37
NC_000002.10:g.21087388G>C NCBI36
NG_011793.1:g.38063C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5857C>G MANE Select ENSP00000233242.1:p.His1953Asp
ENST00000616098.4:c.5857C>G ENSP00000477990.1:p.His1953Asp
NM_000384.2:c.5857C>G NP_000375.2:p.His1953Asp
XM_011532809.1:c.5857C>G XP_011531111.1:p.His1953Asp
NM_000384.3:c.5857C>G MANE Select NP_000375.3:p.His1953Asp