Canonical Allele Identifier: CA2271193170
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66231148A= , CM000679.2:g.66231148A= GRCh38
NC_000017.10:g.64227266A= , CM000679.1:g.64227266A= GRCh37
NC_000017.9:g.61657728A= NCBI36
NG_012045.1:g.3291T=

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-1726T= ENSP00000464301.1:n.-43-1726T=