Canonical Allele Identifier: CA406301506
Gene: APOE HGNC NCBI

Linked Data

gnomAD v4: 19-44905924-G-A
MyVariant Identifiers: chr19:g.45409181G>A (hg19) chr19:g.44905924G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44905924G>A , CM000681.2:g.44905924G>A GRCh38
NC_000019.9:g.45409181G>A , CM000681.1:g.45409181G>A GRCh37
NC_000019.8:g.50101021G>A NCBI36
NG_007084.2:g.5143G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252486.9:c.-24+83G>A MANE Select ENSP00000252486.3:n.-24+83G>A
ENST00000252486.8:c.-24+83G>A ENSP00000252486.3:n.-24+83G>A
ENST00000434152.5:c.55+1G>A ENSP00000413653.2:n.55+1G>A
ENST00000446996.5:c.-39+83G>A ENSP00000413135.1:n.-39+83G>A
ENST00000485628.2:n.46+83G>A
NM_000041.3:c.-24+83G>A NP_000032.1:n.-24+83G>A
NM_001302688.1:c.55+1G>A NP_001289617.1:n.55+1G>A
NM_001302691.1:c.-39+83G>A NP_001289620.1:n.-39+83G>A
NM_000041.4:c.-24+83G>A MANE Select NP_000032.1:n.-24+83G>A
NM_001302688.2:c.55+1G>A NP_001289617.1:n.55+1G>A
NM_001302691.2:c.-39+83G>A NP_001289620.1:n.-39+83G>A
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