Canonical Allele Identifier: CA400683861
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1233203452

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228121A>G , CM000679.2:g.66228121A>G GRCh38
NC_000017.10:g.64224239A>G , CM000679.1:g.64224239A>G GRCh37
NC_000017.9:g.61654701A>G NCBI36
NG_012045.1:g.6318T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.140T>C MANE Select ENSP00000205948.6:p.Ile47Thr
ENST00000205948.10:c.140T>C ENSP00000205948.6:p.Ile47Thr
ENST00000577982.1:c.140T>C ENSP00000464301.1:p.Ile47Thr
ENST00000581797.5:c.-41T>C ENSP00000463553.1:n.-41T>C
NM_000042.2:c.140T>C NP_000033.2:p.Ile47Thr
NM_000042.3:c.140T>C MANE Select NP_000033.2:p.Ile47Thr