Canonical Allele Identifier: CA425346608
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1663314842
MyVariant Identifiers: chr2:g.21234190G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011318G>A , CM000664.2:g.21011318G>A GRCh38
NC_000002.11:g.21234190G>A , CM000664.1:g.21234190G>A GRCh37
NC_000002.10:g.21087695G>A NCBI36
NG_011793.1:g.37756C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5550C>T MANE Select ENSP00000233242.1:p.Ser1850=
ENST00000616098.4:c.5550C>T ENSP00000477990.1:p.Ser1850=
NM_000384.2:c.5550C>T NP_000375.2:p.Ser1850=
XM_011532809.1:c.5550C>T XP_011531111.1:p.Ser1850=
NM_000384.3:c.5550C>T MANE Select NP_000375.3:p.Ser1850=
Search 100 bp 5'
Search 100 bp 3'