Canonical Allele Identifier: CA996247942

Gene: APOE

Linked Data

• dbSNP Id: rs938557696
• gnomAD v3: 19-44909354-G-T
• gnomAD v4: 19-44909354-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909354G>T , CM000681.2:g.44909354G>T	GRCh38
NC_000019.9:g.45412611G>T , CM000681.1:g.45412611G>T	GRCh37
NC_000019.8:g.50104451G>T	NCBI36
NG_007084.2:g.8573G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.*104G>T MANE Select	ENSP00000252486.3:n.*104G>T
ENST00000252486.8:c.*104G>T	ENSP00000252486.3:n.*104G>T
NM_000041.3:c.*104G>T	NP_000032.1:n.*104G>T
NM_001302688.1:c.*104G>T	NP_001289617.1:n.*104G>T
NM_001302689.1:c.*104G>T	NP_001289618.1:n.*104G>T
NM_001302690.1:c.*104G>T	NP_001289619.1:n.*104G>T
NM_001302691.1:c.*104G>T	NP_001289620.1:n.*104G>T
NM_000041.4:c.*104G>T MANE Select	NP_000032.1:n.*104G>T
NM_001302688.2:c.*104G>T	NP_001289617.1:n.*104G>T
NM_001302689.2:c.*104G>T	NP_001289618.1:n.*104G>T
NM_001302691.2:c.*104G>T	NP_001289620.1:n.*104G>T
NM_001302690.2:c.*104G>T	NP_001289619.1:n.*104G>T