Canonical Allele Identifier: CA400683741
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228061G>T , CM000679.2:g.66228061G>T GRCh38
NC_000017.10:g.64224179G>T , CM000679.1:g.64224179G>T GRCh37
NC_000017.9:g.61654641G>T NCBI36
NG_012045.1:g.6378C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.200C>A MANE Select ENSP00000205948.6:p.Pro67His
ENST00000205948.10:c.200C>A ENSP00000205948.6:p.Pro67His
ENST00000577982.1:c.200C>A ENSP00000464301.1:p.Pro67His
ENST00000581797.5:c.20C>A ENSP00000463553.1:p.Pro7His
NM_000042.2:c.200C>A NP_000033.2:p.Pro67His
NM_000042.3:c.200C>A MANE Select NP_000033.2:p.Pro67His