Canonical Allele Identifier: CA501476114
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224207G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228089G>T , CM000679.2:g.66228089G>T GRCh38
NC_000017.10:g.64224207G>T , CM000679.1:g.64224207G>T GRCh37
NC_000017.9:g.61654669G>T NCBI36
NG_012045.1:g.6350C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.172C>A MANE Select ENSP00000205948.6:p.Arg58=
ENST00000205948.10:c.172C>A ENSP00000205948.6:p.Arg58=
ENST00000577982.1:c.172C>A ENSP00000464301.1:p.Arg58=
ENST00000581797.5:c.-9C>A ENSP00000463553.1:n.-9C>A
NM_000042.2:c.172C>A NP_000033.2:p.Arg58=
NM_000042.3:c.172C>A MANE Select NP_000033.2:p.Arg58=
Search 100 bp 5'
Search 100 bp 3'