Canonical Allele Identifier: CA400683960
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228166G>T , CM000679.2:g.66228166G>T GRCh38
NC_000017.10:g.64224284G>T , CM000679.1:g.64224284G>T GRCh37
NC_000017.9:g.61654746G>T NCBI36
NG_012045.1:g.6273C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.95C>A MANE Select ENSP00000205948.6:p.Ser32Tyr
ENST00000205948.10:c.95C>A ENSP00000205948.6:p.Ser32Tyr
ENST00000577982.1:c.95C>A ENSP00000464301.1:p.Ser32Tyr
ENST00000581797.5:c.-86C>A ENSP00000463553.1:n.-86C>A
NM_000042.2:c.95C>A NP_000033.2:p.Ser32Tyr
NM_000042.3:c.95C>A MANE Select NP_000033.2:p.Ser32Tyr