Canonical Allele Identifier: CA343320424

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192228G>C (hg19) ; chr1:g.161222438G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222438G>C , CM000663.2:g.161222438G>C	GRCh38
NC_000001.10:g.161192228G>C , CM000663.1:g.161192228G>C	GRCh37
NC_000001.9:g.159458852G>C	NCBI36
NG_012043.1:g.6191C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.270C>G MANE Select	ENSP00000356969.3:p.Phe90Leu
ENST00000463273.5:c.270C>G	ENSP00000476740.1:p.Phe90Leu
ENST00000463812.1:c.126C>G	ENSP00000476890.1:p.Phe42Leu
ENST00000464492.5:c.369C>G	ENSP00000476911.1:p.Phe123Leu
ENST00000468465.5:c.126C>G	ENSP00000476662.1:p.Phe42Leu
ENST00000470459.6:c.216C>G	ENSP00000477031.1:p.Phe72Leu
ENST00000481413.1:n.781C>G
ENST00000481511.5:c.*267C>G	ENSP00000477054.1:n.*267C>G
ENST00000491350.1:c.*53C>G	ENSP00000477353.1:n.*53C>G
NM_001643.1:c.270C>G	NP_001634.1:p.Phe90Leu
NM_001643.2:c.270C>G MANE Select	NP_001634.1:p.Phe90Leu