Canonical Allele Identifier: CA43506229
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs778718854
MyVariant Identifiers: chr2:g.21233890T>C (hg19) chr2:g.21011018T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011018T>C , CM000664.2:g.21011018T>C GRCh38
NC_000002.11:g.21233890T>C , CM000664.1:g.21233890T>C GRCh37
NC_000002.10:g.21087395T>C NCBI36
NG_011793.1:g.38056A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5850A>G MANE Select ENSP00000233242.1:p.Thr1950=
ENST00000616098.4:c.5850A>G ENSP00000477990.1:p.Thr1950=
NM_000384.2:c.5850A>G NP_000375.2:p.Thr1950=
XM_011532809.1:c.5850A>G XP_011531111.1:p.Thr1950=
NM_000384.3:c.5850A>G MANE Select NP_000375.3:p.Thr1950=
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