Canonical Allele Identifier: CA507947897
Gene: APOE HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.45412090G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908833G>T , CM000681.2:g.44908833G>T GRCh38
NC_000019.9:g.45412090G>T , CM000681.1:g.45412090G>T GRCh37
NC_000019.8:g.50103930G>T NCBI36
NG_007084.2:g.8052G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252486.9:c.537G>T MANE Select ENSP00000252486.3:p.Val179=
ENST00000252486.8:c.537G>T ENSP00000252486.3:p.Val179=
ENST00000425718.1:c.537G>T ENSP00000410423.1:p.Val179=
ENST00000434152.5:c.615G>T ENSP00000413653.2:p.Val205=
ENST00000446996.5:c.537G>T ENSP00000413135.1:p.Val179=
NM_000041.3:c.537G>T NP_000032.1:p.Val179=
NM_001302688.1:c.615G>T NP_001289617.1:p.Val205=
NM_001302689.1:c.537G>T NP_001289618.1:p.Val179=
NM_001302690.1:c.537G>T NP_001289619.1:p.Val179=
NM_001302691.1:c.537G>T NP_001289620.1:p.Val179=
NM_000041.4:c.537G>T MANE Select NP_000032.1:p.Val179=
NM_001302688.2:c.615G>T NP_001289617.1:p.Val205=
NM_001302689.2:c.537G>T NP_001289618.1:p.Val179=
NM_001302691.2:c.537G>T NP_001289620.1:p.Val179=
NM_001302690.2:c.537G>T NP_001289619.1:p.Val179=