Canonical Allele Identifier: CA400683925
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228148T>C , CM000679.2:g.66228148T>C GRCh38
NC_000017.10:g.64224266T>C , CM000679.1:g.64224266T>C GRCh37
NC_000017.9:g.61654728T>C NCBI36
NG_012045.1:g.6291A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.113A>G MANE Select ENSP00000205948.6:p.Lys38Arg
ENST00000205948.10:c.113A>G ENSP00000205948.6:p.Lys38Arg
ENST00000577982.1:c.113A>G ENSP00000464301.1:p.Lys38Arg
ENST00000581797.5:c.-68A>G ENSP00000463553.1:n.-68A>G
NM_000042.2:c.113A>G NP_000033.2:p.Lys38Arg
NM_000042.3:c.113A>G MANE Select NP_000033.2:p.Lys38Arg