Canonical Allele Identifier: CA501476150
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224238A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228120A>G , CM000679.2:g.66228120A>G GRCh38
NC_000017.10:g.64224238A>G , CM000679.1:g.64224238A>G GRCh37
NC_000017.9:g.61654700A>G NCBI36
NG_012045.1:g.6319T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.141T>C MANE Select ENSP00000205948.6:p.Ile47=
ENST00000205948.10:c.141T>C ENSP00000205948.6:p.Ile47=
ENST00000577982.1:c.141T>C ENSP00000464301.1:p.Ile47=
ENST00000581797.5:c.-40T>C ENSP00000463553.1:n.-40T>C
NM_000042.2:c.141T>C NP_000033.2:p.Ile47=
NM_000042.3:c.141T>C MANE Select NP_000033.2:p.Ile47=
Search 100 bp 5'
Search 100 bp 3'