Canonical Allele Identifier: CA2271191808
Gene: APOH HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.200C= MANE Select ENSP00000205948.6:p.Pro67=
ENST00000205948.10:c.200C= ENSP00000205948.6:p.Pro67=
ENST00000577982.1:c.200C= ENSP00000464301.1:p.Pro67=
ENST00000581797.5:c.20C= ENSP00000463553.1:p.Pro7=
NM_000042.2:c.200C= NP_000033.2:p.Pro67=
NM_000042.3:c.200C= MANE Select NP_000033.2:p.Pro67=