Canonical Allele Identifier: CA346001741
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21233295A>G (hg19) chr2:g.21010423A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010423A>G , CM000664.2:g.21010423A>G GRCh38
NC_000002.11:g.21233295A>G , CM000664.1:g.21233295A>G GRCh37
NC_000002.10:g.21086800A>G NCBI36
NG_011793.1:g.38651T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.6445T>C MANE Select ENSP00000233242.1:p.Tyr2149His
ENST00000616098.4:c.6445T>C ENSP00000477990.1:p.Tyr2149His
NM_000384.2:c.6445T>C NP_000375.2:p.Tyr2149His
XM_011532809.1:c.5869+310T>C XP_011531111.1:n.5869+310T>C
NM_000384.3:c.6445T>C MANE Select NP_000375.3:p.Tyr2149His
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Search 100 bp 3'