Canonical Allele Identifier: CA501476115
Gene: APOH HGNC NCBI

Linked Data

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

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

Transcript Alleles

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