Canonical Allele Identifier: CA400683912
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224260A>T (hg19) chr17:g.66228142A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228142A>T , CM000679.2:g.66228142A>T GRCh38
NC_000017.10:g.64224260A>T , CM000679.1:g.64224260A>T GRCh37
NC_000017.9:g.61654722A>T NCBI36
NG_012045.1:g.6297T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.119T>A MANE Select ENSP00000205948.6:p.Phe40Tyr
ENST00000205948.10:c.119T>A ENSP00000205948.6:p.Phe40Tyr
ENST00000577982.1:c.119T>A ENSP00000464301.1:p.Phe40Tyr
ENST00000581797.5:c.-62T>A ENSP00000463553.1:n.-62T>A
NM_000042.2:c.119T>A NP_000033.2:p.Phe40Tyr
NM_000042.3:c.119T>A MANE Select NP_000033.2:p.Phe40Tyr
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