Canonical Allele Identifier: CA345977128
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21227950A>T (hg19) chr2:g.21005078A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21005078A>T , CM000664.2:g.21005078A>T GRCh38
NC_000002.11:g.21227950A>T , CM000664.1:g.21227950A>T GRCh37
NC_000002.10:g.21081455A>T NCBI36
NG_011793.1:g.43996T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.11788+2T>A MANE Select ENSP00000233242.1:n.11788+2T>A
ENST00000616098.4:c.11788+2T>A ENSP00000477990.1:n.11788+2T>A
NM_000384.2:c.11788+2T>A NP_000375.2:n.11788+2T>A
XM_011532809.1:c.5869+5655T>A XP_011531111.1:n.5869+5655T>A
NM_000384.3:c.11788+2T>A MANE Select NP_000375.3:n.11788+2T>A
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