Canonical Allele Identifier: CA501476117
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224208G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228090G>T , CM000679.2:g.66228090G>T GRCh38
NC_000017.10:g.64224208G>T , CM000679.1:g.64224208G>T GRCh37
NC_000017.9:g.61654670G>T NCBI36
NG_012045.1:g.6349C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.171C>A MANE Select ENSP00000205948.6:p.Ser57=
ENST00000205948.10:c.171C>A ENSP00000205948.6:p.Ser57=
ENST00000577982.1:c.171C>A ENSP00000464301.1:p.Ser57=
ENST00000581797.5:c.-10C>A ENSP00000463553.1:n.-10C>A
NM_000042.2:c.171C>A NP_000033.2:p.Ser57=
NM_000042.3:c.171C>A MANE Select NP_000033.2:p.Ser57=
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