Canonical Allele Identifier: CA346003859
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1394574014
MyVariant Identifiers: chr2:g.21233898C>T (hg19) chr2:g.21011026C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011026C>T , CM000664.2:g.21011026C>T GRCh38
NC_000002.11:g.21233898C>T , CM000664.1:g.21233898C>T GRCh37
NC_000002.10:g.21087403C>T NCBI36
NG_011793.1:g.38048G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5842G>A MANE Select ENSP00000233242.1:p.Gly1948Ser
ENST00000616098.4:c.5842G>A ENSP00000477990.1:p.Gly1948Ser
NM_000384.2:c.5842G>A NP_000375.2:p.Gly1948Ser
XM_011532809.1:c.5842G>A XP_011531111.1:p.Gly1948Ser
NM_000384.3:c.5842G>A MANE Select NP_000375.3:p.Gly1948Ser
Search 100 bp 5'
Search 100 bp 3'