Canonical Allele Identifier: CA345997606
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21009634-A-G
MyVariant Identifiers: chr2:g.21232506A>G (hg19) chr2:g.21009634A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009634A>G , CM000664.2:g.21009634A>G GRCh38
NC_000002.11:g.21232506A>G , CM000664.1:g.21232506A>G GRCh37
NC_000002.10:g.21086011A>G NCBI36
NG_011793.1:g.39440T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.7234T>C MANE Select ENSP00000233242.1:p.Phe2412Leu
ENST00000616098.4:c.7234T>C ENSP00000477990.1:p.Phe2412Leu
NM_000384.2:c.7234T>C NP_000375.2:p.Phe2412Leu
XM_011532809.1:c.5869+1099T>C XP_011531111.1:n.5869+1099T>C
NM_000384.3:c.7234T>C MANE Select NP_000375.3:p.Phe2412Leu
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