Canonical Allele Identifier: CA2658074503
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21005068-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21005068G>C , CM000664.2:g.21005068G>C GRCh38
NC_000002.11:g.21227940G>C , CM000664.1:g.21227940G>C GRCh37
NC_000002.10:g.21081445G>C NCBI36
NG_011793.1:g.44006C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.11788+12C>G MANE Select ENSP00000233242.1:n.11788+12C>G
ENST00000616098.4:c.11788+12C>G ENSP00000477990.1:n.11788+12C>G
NM_000384.2:c.11788+12C>G NP_000375.2:n.11788+12C>G
XM_011532809.1:c.5869+5665C>G XP_011531111.1:n.5869+5665C>G
NM_000384.3:c.11788+12C>G MANE Select NP_000375.3:n.11788+12C>G
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