Canonical Allele Identifier: CA345968358
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21225077T>G (hg19) chr2:g.21002205T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002205T>G , CM000664.2:g.21002205T>G GRCh38
NC_000002.11:g.21225077T>G , CM000664.1:g.21225077T>G GRCh37
NC_000002.10:g.21078582T>G NCBI36
NG_011793.1:g.46869A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13217A>C MANE Select ENSP00000233242.1:p.Lys4406Thr
ENST00000616098.4:c.13215A>C ENSP00000477990.1:n.13215A>C
NM_000384.2:c.13217A>C NP_000375.2:p.Lys4406Thr
XM_011532809.1:c.5870-2932A>C XP_011531111.1:n.5870-2932A>C
NM_000384.3:c.13217A>C MANE Select NP_000375.3:p.Lys4406Thr
Search 100 bp 5'
Search 100 bp 3'