Canonical Allele Identifier: CA400683727
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228053C>T , CM000679.2:g.66228053C>T GRCh38
NC_000017.10:g.64224171C>T , CM000679.1:g.64224171C>T GRCh37
NC_000017.9:g.61654633C>T NCBI36
NG_012045.1:g.6386G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.208G>A MANE Select ENSP00000205948.6:p.Gly70Arg
ENST00000205948.10:c.208G>A ENSP00000205948.6:p.Gly70Arg
ENST00000577982.1:c.208G>A ENSP00000464301.1:p.Gly70Arg
ENST00000581797.5:c.28G>A ENSP00000463553.1:p.Gly10Arg
NM_000042.2:c.208G>A NP_000033.2:p.Gly70Arg
NM_000042.3:c.208G>A MANE Select NP_000033.2:p.Gly70Arg