Canonical Allele Identifier: CA501476158
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224250T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228132T>G , CM000679.2:g.66228132T>G GRCh38
NC_000017.10:g.64224250T>G , CM000679.1:g.64224250T>G GRCh37
NC_000017.9:g.61654712T>G NCBI36
NG_012045.1:g.6307A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.129A>C MANE Select ENSP00000205948.6:p.Pro43=
ENST00000205948.10:c.129A>C ENSP00000205948.6:p.Pro43=
ENST00000577982.1:c.129A>C ENSP00000464301.1:p.Pro43=
ENST00000581797.5:c.-52A>C ENSP00000463553.1:n.-52A>C
NM_000042.2:c.129A>C NP_000033.2:p.Pro43=
NM_000042.3:c.129A>C MANE Select NP_000033.2:p.Pro43=
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