Canonical Allele Identifier: CA8720521
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs755547171
ExAC: 17:64224295 A / T
gnomAD v2: 17-64224295-A-T
gnomAD v4: 17-66228177-A-T
MyVariant Identifiers: chr17:g.64224295A>T (hg19) chr17:g.66228177A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228177A>T , CM000679.2:g.66228177A>T GRCh38
NC_000017.10:g.64224295A>T , CM000679.1:g.64224295A>T GRCh37
NC_000017.9:g.61654757A>T NCBI36
NG_012045.1:g.6262T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.84T>A MANE Select ENSP00000205948.6:p.Asp28Glu
ENST00000205948.10:c.84T>A ENSP00000205948.6:p.Asp28Glu
ENST00000577982.1:c.84T>A ENSP00000464301.1:p.Asp28Glu
ENST00000581797.5:c.-97T>A ENSP00000463553.1:n.-97T>A
NM_000042.2:c.84T>A NP_000033.2:p.Asp28Glu
NM_000042.3:c.84T>A MANE Select NP_000033.2:p.Asp28Glu
Search 100 bp 5'
Search 100 bp 3'