Canonical Allele Identifier: CA43487650
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs900908225
MyVariant Identifiers: chr2:g.21224900T>C (hg19) chr2:g.21002028T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002028T>C , CM000664.2:g.21002028T>C GRCh38
NC_000002.11:g.21224900T>C , CM000664.1:g.21224900T>C GRCh37
NC_000002.10:g.21078405T>C NCBI36
NG_011793.1:g.47046A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13394A>G MANE Select ENSP00000233242.1:p.Lys4465Arg
ENST00000616098.4:c.13392A>G ENSP00000477990.1:n.13392A>G
NM_000384.2:c.13394A>G NP_000375.2:p.Lys4465Arg
XM_011532809.1:c.5870-2755A>G XP_011531111.1:n.5870-2755A>G
NM_000384.3:c.13394A>G MANE Select NP_000375.3:p.Lys4465Arg
Search 100 bp 5'
Search 100 bp 3'