Canonical Allele Identifier: CA062626
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs772786000
ExAC: 2:21233810 TG / T
gnomAD v2: 2-21233810-TG-T
gnomAD v4: 2-21010938-TG-T
MyVariant Identifiers: chr2:g.21233811del (hg19) chr2:g.21010939del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010939del , CM000664.2:g.21010939del GRCh38
NC_000002.11:g.21233811del , CM000664.1:g.21233811del GRCh37
NC_000002.10:g.21087316del NCBI36
NG_011793.1:g.38135del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5929del MANE Select ENSP00000233242.1:p.Gln1977ArgfsTer?
ENST00000616098.4:c.5929del ENSP00000477990.1:p.Gln1977ArgfsTer?
NM_000384.2:c.5929del NP_000375.2:p.Gln1977ArgfsTer?
XM_011532809.1:c.5864+65del XP_011531111.1:n.5864+65del
NM_000384.3:c.5929del MANE Select NP_000375.3:p.Gln1977ArgfsTer?
Search 100 bp 5'
Search 100 bp 3'