Canonical Allele Identifier: CA43487252
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs769181415
MyVariant Identifiers: chr2:g.21001692T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001692T>A , CM000664.2:g.21001692T>A GRCh38
NC_000002.11:g.21224564T>A , CM000664.1:g.21224564T>A GRCh37
NC_000002.10:g.21078069T>A NCBI36
NG_011793.1:g.47382A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.*38A>T MANE Select ENSP00000233242.1:n.*38A>T
ENST00000616098.4:c.13728A>T ENSP00000477990.1:n.13728A>T
NM_000384.2:c.*38A>T NP_000375.2:n.*38A>T
XM_011532809.1:c.5870-2419A>T XP_011531111.1:n.5870-2419A>T
NM_000384.3:c.*38A>T MANE Select NP_000375.3:n.*38A>T