Canonical Allele Identifier: CA2573939445
Gene: APOA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161222588T>A , CM000663.2:g.161222588T>A GRCh38
NC_000001.10:g.161192378T>A , CM000663.1:g.161192378T>A GRCh37
NC_000001.9:g.159459002T>A NCBI36
NG_012043.1:g.6041A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367990.7:c.186-66A>T MANE Select ENSP00000356969.3:n.186-66A>T
ENST00000463273.5:c.186-66A>T ENSP00000476740.1:n.186-66A>T
ENST00000463812.1:c.42-66A>T ENSP00000476890.1:n.42-66A>T
ENST00000464492.5:c.285-66A>T ENSP00000476911.1:n.285-66A>T
ENST00000468465.5:c.42-66A>T ENSP00000476662.1:n.42-66A>T
ENST00000469730.2:c.186-66A>T ENSP00000476605.1:n.186-66A>T
ENST00000470459.6:c.186-66A>T ENSP00000477031.1:n.186-66A>T
ENST00000481413.1:n.697-66A>T
ENST00000481511.5:c.*183-66A>T ENSP00000477054.1:n.*183-66A>T
ENST00000491350.1:c.53-66A>T ENSP00000477353.1:n.53-66A>T
NM_001643.1:c.186-66A>T NP_001634.1:n.186-66A>T
NM_001643.2:c.186-66A>T MANE Select NP_001634.1:n.186-66A>T