Canonical Allele Identifier: CA507947653
Gene: APOE HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.45411991G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908734G>A , CM000681.2:g.44908734G>A GRCh38
NC_000019.9:g.45411991G>A , CM000681.1:g.45411991G>A GRCh37
NC_000019.8:g.50103831G>A NCBI36
NG_007084.2:g.7953G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252486.9:c.438G>A MANE Select ENSP00000252486.3:p.Gln146=
ENST00000252486.8:c.438G>A ENSP00000252486.3:p.Gln146=
ENST00000425718.1:c.438G>A ENSP00000410423.1:p.Gln146=
ENST00000434152.5:c.516G>A ENSP00000413653.2:p.Gln172=
ENST00000446996.5:c.438G>A ENSP00000413135.1:p.Gln146=
NM_000041.3:c.438G>A NP_000032.1:p.Gln146=
NM_001302688.1:c.516G>A NP_001289617.1:p.Gln172=
NM_001302689.1:c.438G>A NP_001289618.1:p.Gln146=
NM_001302690.1:c.438G>A NP_001289619.1:p.Gln146=
NM_001302691.1:c.438G>A NP_001289620.1:p.Gln146=
NM_000041.4:c.438G>A MANE Select NP_000032.1:p.Gln146=
NM_001302688.2:c.516G>A NP_001289617.1:p.Gln172=
NM_001302689.2:c.438G>A NP_001289618.1:p.Gln146=
NM_001302691.2:c.438G>A NP_001289620.1:p.Gln146=
NM_001302690.2:c.438G>A NP_001289619.1:p.Gln146=