Canonical Allele Identifier: CA425343928
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21229699G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21006827G>T , CM000664.2:g.21006827G>T GRCh38
NC_000002.11:g.21229699G>T , CM000664.1:g.21229699G>T GRCh37
NC_000002.10:g.21083204G>T NCBI36
NG_011793.1:g.42247C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.10041C>A MANE Select ENSP00000233242.1:p.Val3347=
ENST00000616098.4:c.10041C>A ENSP00000477990.1:p.Val3347=
NM_000384.2:c.10041C>A NP_000375.2:p.Val3347=
XM_011532809.1:c.5869+3906C>A XP_011531111.1:n.5869+3906C>A
NM_000384.3:c.10041C>A MANE Select NP_000375.3:p.Val3347=
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Search 100 bp 3'