Canonical Allele Identifier: CA501476126
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224217G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228099G>C , CM000679.2:g.66228099G>C GRCh38
NC_000017.10:g.64224217G>C , CM000679.1:g.64224217G>C GRCh37
NC_000017.9:g.61654679G>C NCBI36
NG_012045.1:g.6340C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.162C>G MANE Select ENSP00000205948.6:p.Gly54=
ENST00000205948.10:c.162C>G ENSP00000205948.6:p.Gly54=
ENST00000577982.1:c.162C>G ENSP00000464301.1:p.Gly54=
ENST00000581797.5:c.-19C>G ENSP00000463553.1:n.-19C>G
NM_000042.2:c.162C>G NP_000033.2:p.Gly54=
NM_000042.3:c.162C>G MANE Select NP_000033.2:p.Gly54=
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