Canonical Allele Identifier: CA425346347
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21233929A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011057A>C , CM000664.2:g.21011057A>C GRCh38
NC_000002.11:g.21233929A>C , CM000664.1:g.21233929A>C GRCh37
NC_000002.10:g.21087434A>C NCBI36
NG_011793.1:g.38017T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5811T>G MANE Select ENSP00000233242.1:p.Pro1937=
ENST00000616098.4:c.5811T>G ENSP00000477990.1:p.Pro1937=
NM_000384.2:c.5811T>G NP_000375.2:p.Pro1937=
XM_011532809.1:c.5811T>G XP_011531111.1:p.Pro1937=
NM_000384.3:c.5811T>G MANE Select NP_000375.3:p.Pro1937=