Canonical Allele Identifier: CA343320436

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192231A>C (hg19) ; chr1:g.161222441A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222441A>C , CM000663.2:g.161222441A>C	GRCh38
NC_000001.10:g.161192231A>C , CM000663.1:g.161192231A>C	GRCh37
NC_000001.9:g.159458855A>C	NCBI36
NG_012043.1:g.6188T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.267T>G MANE Select	ENSP00000356969.3:p.Tyr89Ter
ENST00000463273.5:c.267T>G	ENSP00000476740.1:p.Tyr89Ter
ENST00000463812.1:c.123T>G	ENSP00000476890.1:p.Tyr41Ter
ENST00000464492.5:c.366T>G	ENSP00000476911.1:p.Tyr122Ter
ENST00000468465.5:c.123T>G	ENSP00000476662.1:p.Tyr41Ter
ENST00000470459.6:c.213T>G	ENSP00000477031.1:p.Tyr71Ter
ENST00000481413.1:n.778T>G
ENST00000481511.5:c.*264T>G	ENSP00000477054.1:n.*264T>G
ENST00000491350.1:c.*50T>G	ENSP00000477353.1:n.*50T>G
NM_001643.1:c.267T>G	NP_001634.1:p.Tyr89Ter
NM_001643.2:c.267T>G MANE Select	NP_001634.1:p.Tyr89Ter