Canonical Allele Identifier: CA346003910
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21011049-A-G
MyVariant Identifiers: chr2:g.21233921A>G (hg19) chr2:g.21011049A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011049A>G , CM000664.2:g.21011049A>G GRCh38
NC_000002.11:g.21233921A>G , CM000664.1:g.21233921A>G GRCh37
NC_000002.10:g.21087426A>G NCBI36
NG_011793.1:g.38025T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5819T>C MANE Select ENSP00000233242.1:p.Phe1940Ser
ENST00000616098.4:c.5819T>C ENSP00000477990.1:p.Phe1940Ser
NM_000384.2:c.5819T>C NP_000375.2:p.Phe1940Ser
XM_011532809.1:c.5819T>C XP_011531111.1:p.Phe1940Ser
NM_000384.3:c.5819T>C MANE Select NP_000375.3:p.Phe1940Ser
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