Canonical Allele Identifier: CA400683855
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228119T>A , CM000679.2:g.66228119T>A GRCh38
NC_000017.10:g.64224237T>A , CM000679.1:g.64224237T>A GRCh37
NC_000017.9:g.61654699T>A NCBI36
NG_012045.1:g.6320A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.142A>T MANE Select ENSP00000205948.6:p.Thr48Ser
ENST00000205948.10:c.142A>T ENSP00000205948.6:p.Thr48Ser
ENST00000577982.1:c.142A>T ENSP00000464301.1:p.Thr48Ser
ENST00000581797.5:c.-39A>T ENSP00000463553.1:n.-39A>T
NM_000042.2:c.142A>T NP_000033.2:p.Thr48Ser
NM_000042.3:c.142A>T MANE Select NP_000033.2:p.Thr48Ser