Canonical Allele Identifier: CA343320703

Gene: APOA2

Linked Data

• gnomAD v4: 1-161222494-G-C
• MyVariant Identifiers: chr1:g.161192284G>C (hg19) ; chr1:g.161222494G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222494G>C , CM000663.2:g.161222494G>C	GRCh38
NC_000001.10:g.161192284G>C , CM000663.1:g.161192284G>C	GRCh37
NC_000001.9:g.159458908G>C	NCBI36
NG_012043.1:g.6135C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.214C>G MANE Select	ENSP00000356969.3:p.Leu72Val
ENST00000463273.5:c.214C>G	ENSP00000476740.1:p.Leu72Val
ENST00000463812.1:c.70C>G	ENSP00000476890.1:p.Leu24Val
ENST00000464492.5:c.313C>G	ENSP00000476911.1:p.Leu105Val
ENST00000468465.5:c.70C>G	ENSP00000476662.1:p.Leu24Val
ENST00000470459.6:c.200+14C>G	ENSP00000477031.1:n.200+14C>G
ENST00000481413.1:n.725C>G
ENST00000481511.5:c.*211C>G	ENSP00000477054.1:n.*211C>G
ENST00000491350.1:c.81C>G	ENSP00000477353.1:p.Ser27Arg
NM_001643.1:c.214C>G	NP_001634.1:p.Leu72Val
NM_001643.2:c.214C>G MANE Select	NP_001634.1:p.Leu72Val