Canonical Allele Identifier: CA425347201
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21238050G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21015178G>C , CM000664.2:g.21015178G>C GRCh38
NC_000002.11:g.21238050G>C , CM000664.1:g.21238050G>C GRCh37
NC_000002.10:g.21091555G>C NCBI36
NG_011793.1:g.33896C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.2:c.*2897C>G ENSP00000501110.2:n.*2897C>G
ENST00000673882.2:c.*2686C>G ENSP00000501253.2:n.*2686C>G
ENST00000673739.1:c.3305C>G ENSP00000501110.1:n.3305C>G
ENST00000673882.1:c.3094C>G ENSP00000501253.1:n.3094C>G
ENST00000233242.5:c.3591C>G MANE Select ENSP00000233242.1:p.Leu1197=
ENST00000616098.4:c.3591C>G ENSP00000477990.1:p.Leu1197=
NM_000384.2:c.3591C>G NP_000375.2:p.Leu1197=
XM_011532809.1:c.3591C>G XP_011531111.1:p.Leu1197=
NM_000384.3:c.3591C>G MANE Select NP_000375.3:p.Leu1197=
Search 100 bp 5'
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