Canonical Allele Identifier: CA346007654
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21236160T>G (hg19) chr2:g.21013288T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21013288T>G , CM000664.2:g.21013288T>G GRCh38
NC_000002.11:g.21236160T>G , CM000664.1:g.21236160T>G GRCh37
NC_000002.10:g.21089665T>G NCBI36
NG_011793.1:g.35786A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.2:c.*3394A>C ENSP00000501110.2:n.*3394A>C
ENST00000673739.1:c.3802A>C ENSP00000501110.1:n.3802A>C
ENST00000233242.5:c.4088A>C MANE Select ENSP00000233242.1:p.Tyr1363Ser
ENST00000616098.4:c.4088A>C ENSP00000477990.1:p.Tyr1363Ser
NM_000384.2:c.4088A>C NP_000375.2:p.Tyr1363Ser
XM_011532809.1:c.4088A>C XP_011531111.1:p.Tyr1363Ser
NM_000384.3:c.4088A>C MANE Select NP_000375.3:p.Tyr1363Ser
Search 100 bp 5'
Search 100 bp 3'