Canonical Allele Identifier: CA343320622

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192267C>A (hg19) ; chr1:g.161222477C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222477C>A , CM000663.2:g.161222477C>A	GRCh38
NC_000001.10:g.161192267C>A , CM000663.1:g.161192267C>A	GRCh37
NC_000001.9:g.159458891C>A	NCBI36
NG_012043.1:g.6152G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.231G>T MANE Select	ENSP00000356969.3:p.Lys77Asn
ENST00000463273.5:c.231G>T	ENSP00000476740.1:p.Lys77Asn
ENST00000463812.1:c.87G>T	ENSP00000476890.1:p.Lys29Asn
ENST00000464492.5:c.330G>T	ENSP00000476911.1:p.Lys110Asn
ENST00000468465.5:c.87G>T	ENSP00000476662.1:p.Lys29Asn
ENST00000470459.6:c.201-24G>T	ENSP00000477031.1:n.201-24G>T
ENST00000481413.1:n.742G>T
ENST00000481511.5:c.*228G>T	ENSP00000477054.1:n.*228G>T
ENST00000491350.1:c.*14G>T	ENSP00000477353.1:n.*14G>T
NM_001643.1:c.231G>T	NP_001634.1:p.Lys77Asn
NM_001643.2:c.231G>T MANE Select	NP_001634.1:p.Lys77Asn