Canonical Allele Identifier: CA1202652271
Gene: APOA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161222329A= , CM000663.2:g.161222329A= GRCh38
NC_000001.10:g.161192119A= , CM000663.1:g.161192119A= GRCh37
NC_000001.9:g.159458743A= NCBI36
NG_012043.1:g.6300T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367990.7:c.*76T= MANE Select ENSP00000356969.3:n.*76T=
ENST00000463812.1:c.*76T= ENSP00000476890.1:n.*76T=
ENST00000464492.5:c.*76T= ENSP00000476911.1:n.*76T=
ENST00000468465.5:c.*76T= ENSP00000476662.1:n.*76T=
ENST00000470459.6:c.*76T= ENSP00000477031.1:n.*76T=
ENST00000481413.1:n.890T=
ENST00000481511.5:c.*376T= ENSP00000477054.1:n.*376T=
ENST00000491350.1:c.*162T= ENSP00000477353.1:n.*162T=
NM_001643.1:c.*76T= NP_001634.1:n.*76T=
NM_001643.2:c.*76T= MANE Select NP_001634.1:n.*76T=