Canonical Allele Identifier: CA400683830
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228107T>C , CM000679.2:g.66228107T>C GRCh38
NC_000017.10:g.64224225T>C , CM000679.1:g.64224225T>C GRCh37
NC_000017.9:g.61654687T>C NCBI36
NG_012045.1:g.6332A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.154A>G MANE Select ENSP00000205948.6:p.Lys52Glu
ENST00000205948.10:c.154A>G ENSP00000205948.6:p.Lys52Glu
ENST00000577982.1:c.154A>G ENSP00000464301.1:p.Lys52Glu
ENST00000581797.5:c.-27A>G ENSP00000463553.1:n.-27A>G
NM_000042.2:c.154A>G NP_000033.2:p.Lys52Glu
NM_000042.3:c.154A>G MANE Select NP_000033.2:p.Lys52Glu