Canonical Allele Identifier: CA345988429
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21229875C>T (hg19) chr2:g.21007003C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007003C>T , CM000664.2:g.21007003C>T GRCh38
NC_000002.11:g.21229875C>T , CM000664.1:g.21229875C>T GRCh37
NC_000002.10:g.21083380C>T NCBI36
NG_011793.1:g.42071G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9865G>A MANE Select ENSP00000233242.1:p.Asp3289Asn
ENST00000616098.4:c.9865G>A ENSP00000477990.1:p.Asp3289Asn
NM_000384.2:c.9865G>A NP_000375.2:p.Asp3289Asn
XM_011532809.1:c.5869+3730G>A XP_011531111.1:n.5869+3730G>A
NM_000384.3:c.9865G>A MANE Select NP_000375.3:p.Asp3289Asn
Search 100 bp 5'
Search 100 bp 3'