Canonical Allele Identifier: CA062573
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs775995651
ExAC: 2:21233876 A / G
gnomAD v2: 2-21233876-A-G
gnomAD v3: 2-21011004-A-G
gnomAD v4: 2-21011004-A-G
MyVariant Identifiers: chr2:g.21233876A>G (hg19) chr2:g.21011004A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011004A>G , CM000664.2:g.21011004A>G GRCh38
NC_000002.11:g.21233876A>G , CM000664.1:g.21233876A>G GRCh37
NC_000002.10:g.21087381A>G NCBI36
NG_011793.1:g.38070T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5864T>C MANE Select ENSP00000233242.1:p.Val1955Ala
ENST00000616098.4:c.5864T>C ENSP00000477990.1:p.Val1955Ala
NM_000384.2:c.5864T>C NP_000375.2:p.Val1955Ala
XM_011532809.1:c.5864T>C XP_011531111.1:p.Val1955Ala
NM_000384.3:c.5864T>C MANE Select NP_000375.3:p.Val1955Ala
Search 100 bp 5'
Search 100 bp 3'