Canonical Allele Identifier: CA400683969
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224288A>G (hg19) chr17:g.66228170A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228170A>G , CM000679.2:g.66228170A>G GRCh38
NC_000017.10:g.64224288A>G , CM000679.1:g.64224288A>G GRCh37
NC_000017.9:g.61654750A>G NCBI36
NG_012045.1:g.6269T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.91T>C MANE Select ENSP00000205948.6:p.Phe31Leu
ENST00000205948.10:c.91T>C ENSP00000205948.6:p.Phe31Leu
ENST00000577982.1:c.91T>C ENSP00000464301.1:p.Phe31Leu
ENST00000581797.5:c.-90T>C ENSP00000463553.1:n.-90T>C
NM_000042.2:c.91T>C NP_000033.2:p.Phe31Leu
NM_000042.3:c.91T>C MANE Select NP_000033.2:p.Phe31Leu
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