Canonical Allele Identifier: CA501476077
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224181G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228063G>A , CM000679.2:g.66228063G>A GRCh38
NC_000017.10:g.64224181G>A , CM000679.1:g.64224181G>A GRCh37
NC_000017.9:g.61654643G>A NCBI36
NG_012045.1:g.6376C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.198C>T MANE Select ENSP00000205948.6:p.Cys66=
ENST00000205948.10:c.198C>T ENSP00000205948.6:p.Cys66=
ENST00000577982.1:c.198C>T ENSP00000464301.1:p.Cys66=
ENST00000581797.5:c.18C>T ENSP00000463553.1:p.Cys6=
NM_000042.2:c.198C>T NP_000033.2:p.Cys66=
NM_000042.3:c.198C>T MANE Select NP_000033.2:p.Cys66=