Canonical Allele Identifier: CA425346247
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1663300240
MyVariant Identifiers: chr2:g.21233872A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011000A>G , CM000664.2:g.21011000A>G GRCh38
NC_000002.11:g.21233872A>G , CM000664.1:g.21233872A>G GRCh37
NC_000002.10:g.21087377A>G NCBI36
NG_011793.1:g.38074T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5868T>C MANE Select ENSP00000233242.1:p.Ser1956=
ENST00000616098.4:c.5868T>C ENSP00000477990.1:p.Ser1956=
NM_000384.2:c.5868T>C NP_000375.2:p.Ser1956=
XM_011532809.1:c.5864+4T>C XP_011531111.1:n.5864+4T>C
NM_000384.3:c.5868T>C MANE Select NP_000375.3:p.Ser1956=
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Search 100 bp 3'