Canonical Allele Identifier: CA345966888
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21001789-T-C
MyVariant Identifiers: chr2:g.21224661T>C (hg19) chr2:g.21001789T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001789T>C , CM000664.2:g.21001789T>C GRCh38
NC_000002.11:g.21224661T>C , CM000664.1:g.21224661T>C GRCh37
NC_000002.10:g.21078166T>C NCBI36
NG_011793.1:g.47285A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13633A>G MANE Select ENSP00000233242.1:p.Thr4545Ala
ENST00000616098.4:c.13631A>G ENSP00000477990.1:n.13631A>G
NM_000384.2:c.13633A>G NP_000375.2:p.Thr4545Ala
XM_011532809.1:c.5870-2516A>G XP_011531111.1:n.5870-2516A>G
NM_000384.3:c.13633A>G MANE Select NP_000375.3:p.Thr4545Ala
Search 100 bp 5'
Search 100 bp 3'