Canonical Allele Identifier: CA063363
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 630288
ClinVar RCV Id: RCV002536700 RCV003128693
dbSNP Id: rs766444813
ExAC: 2:21233168 A / G
gnomAD v2: 2-21233168-A-G
gnomAD v3: 2-21010296-A-G
gnomAD v4: 2-21010296-A-G
MyVariant Identifiers: chr2:g.21233168A>G (hg19) chr2:g.21010296A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010296A>G , CM000664.2:g.21010296A>G GRCh38
NC_000002.11:g.21233168A>G , CM000664.1:g.21233168A>G GRCh37
NC_000002.10:g.21086673A>G NCBI36
NG_011793.1:g.38778T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6572T>C MANE Select ENSP00000233242.1:p.Leu2191Ser
ENST00000616098.4:c.6572T>C ENSP00000477990.1:p.Leu2191Ser
NM_000384.2:c.6572T>C NP_000375.2:p.Leu2191Ser
XM_011532809.1:c.5869+437T>C XP_011531111.1:n.5869+437T>C
NM_000384.3:c.6572T>C MANE Select NP_000375.3:p.Leu2191Ser
Search 100 bp 5'
Search 100 bp 3'