Canonical Allele Identifier: CA421400212
Gene: APOA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.161192137A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161222347A>G , CM000663.2:g.161222347A>G GRCh38
NC_000001.10:g.161192137A>G , CM000663.1:g.161192137A>G GRCh37
NC_000001.9:g.159458761A>G NCBI36
NG_012043.1:g.6282T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367990.7:c.*58T>C MANE Select ENSP00000356969.3:n.*58T>C
ENST00000463812.1:c.*58T>C ENSP00000476890.1:n.*58T>C
ENST00000464492.5:c.*58T>C ENSP00000476911.1:n.*58T>C
ENST00000468465.5:c.*58T>C ENSP00000476662.1:n.*58T>C
ENST00000470459.6:c.*58T>C ENSP00000477031.1:n.*58T>C
ENST00000481413.1:n.872T>C
ENST00000481511.5:c.*358T>C ENSP00000477054.1:n.*358T>C
ENST00000491350.1:c.*144T>C ENSP00000477353.1:n.*144T>C
NM_001643.1:c.*58T>C NP_001634.1:n.*58T>C
NM_001643.2:c.*58T>C MANE Select NP_001634.1:n.*58T>C
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