Canonical Allele Identifier: CA2585715569

Gene: APOE

Linked Data

• gnomAD v4: 19-44909350-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909350T>C , CM000681.2:g.44909350T>C	GRCh38
NC_000019.9:g.45412607T>C , CM000681.1:g.45412607T>C	GRCh37
NC_000019.8:g.50104447T>C	NCBI36
NG_007084.2:g.8569T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.*100T>C MANE Select	ENSP00000252486.3:n.*100T>C
ENST00000252486.8:c.*100T>C	ENSP00000252486.3:n.*100T>C
NM_000041.3:c.*100T>C	NP_000032.1:n.*100T>C
NM_001302688.1:c.*100T>C	NP_001289617.1:n.*100T>C
NM_001302689.1:c.*100T>C	NP_001289618.1:n.*100T>C
NM_001302690.1:c.*100T>C	NP_001289619.1:n.*100T>C
NM_001302691.1:c.*100T>C	NP_001289620.1:n.*100T>C
NM_000041.4:c.*100T>C MANE Select	NP_000032.1:n.*100T>C
NM_001302688.2:c.*100T>C	NP_001289617.1:n.*100T>C
NM_001302689.2:c.*100T>C	NP_001289618.1:n.*100T>C
NM_001302691.2:c.*100T>C	NP_001289620.1:n.*100T>C
NM_001302690.2:c.*100T>C	NP_001289619.1:n.*100T>C