Canonical Allele Identifier: CA346000200
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21009934-C-A
MyVariant Identifiers: chr2:g.21232806C>A (hg19) chr2:g.21009934C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009934C>A , CM000664.2:g.21009934C>A GRCh38
NC_000002.11:g.21232806C>A , CM000664.1:g.21232806C>A GRCh37
NC_000002.10:g.21086311C>A NCBI36
NG_011793.1:g.39140G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.6934G>T MANE Select ENSP00000233242.1:p.Asp2312Tyr
ENST00000616098.4:c.6934G>T ENSP00000477990.1:p.Asp2312Tyr
NM_000384.2:c.6934G>T NP_000375.2:p.Asp2312Tyr
XM_011532809.1:c.5869+799G>T XP_011531111.1:n.5869+799G>T
NM_000384.3:c.6934G>T MANE Select NP_000375.3:p.Asp2312Tyr
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