Canonical Allele Identifier: CA501476184
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224277C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228159C>A , CM000679.2:g.66228159C>A GRCh38
NC_000017.10:g.64224277C>A , CM000679.1:g.64224277C>A GRCh37
NC_000017.9:g.61654739C>A NCBI36
NG_012045.1:g.6280G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.102G>T MANE Select ENSP00000205948.6:p.Val34=
ENST00000205948.10:c.102G>T ENSP00000205948.6:p.Val34=
ENST00000577982.1:c.102G>T ENSP00000464301.1:p.Val34=
ENST00000581797.5:c.-79G>T ENSP00000463553.1:n.-79G>T
NM_000042.2:c.102G>T NP_000033.2:p.Val34=
NM_000042.3:c.102G>T MANE Select NP_000033.2:p.Val34=
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