Canonical Allele Identifier: CA400683902
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224257T>A (hg19) chr17:g.66228139T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228139T>A , CM000679.2:g.66228139T>A GRCh38
NC_000017.10:g.64224257T>A , CM000679.1:g.64224257T>A GRCh37
NC_000017.9:g.61654719T>A NCBI36
NG_012045.1:g.6300A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.122A>T MANE Select ENSP00000205948.6:p.Tyr41Phe
ENST00000205948.10:c.122A>T ENSP00000205948.6:p.Tyr41Phe
ENST00000577982.1:c.122A>T ENSP00000464301.1:p.Tyr41Phe
ENST00000581797.5:c.-59A>T ENSP00000463553.1:n.-59A>T
NM_000042.2:c.122A>T NP_000033.2:p.Tyr41Phe
NM_000042.3:c.122A>T MANE Select NP_000033.2:p.Tyr41Phe
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