Canonical Allele Identifier: CA421400363
Gene: APOA2 HGNC NCBI

Linked Data

dbSNP Id: rs1571634640
MyVariant Identifiers: chr1:g.161192152T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161222362T>G , CM000663.2:g.161222362T>G GRCh38
NC_000001.10:g.161192152T>G , CM000663.1:g.161192152T>G GRCh37
NC_000001.9:g.159458776T>G NCBI36
NG_012043.1:g.6267A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367990.7:c.*43A>C MANE Select ENSP00000356969.3:n.*43A>C
ENST00000463812.1:c.*43A>C ENSP00000476890.1:n.*43A>C
ENST00000464492.5:c.*43A>C ENSP00000476911.1:n.*43A>C
ENST00000468465.5:c.*43A>C ENSP00000476662.1:n.*43A>C
ENST00000470459.6:c.*43A>C ENSP00000477031.1:n.*43A>C
ENST00000481413.1:n.857A>C
ENST00000481511.5:c.*343A>C ENSP00000477054.1:n.*343A>C
ENST00000491350.1:c.*129A>C ENSP00000477353.1:n.*129A>C
NM_001643.1:c.*43A>C NP_001634.1:n.*43A>C
NM_001643.2:c.*43A>C MANE Select NP_001634.1:n.*43A>C
Search 100 bp 5'
Search 100 bp 3'