Canonical Allele Identifier: CA2271193172
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66231153A= , CM000679.2:g.66231153A= GRCh38
NC_000017.10:g.64227271A= , CM000679.1:g.64227271A= GRCh37
NC_000017.9:g.61657733A= NCBI36
NG_012045.1:g.3286T=

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-1731T= ENSP00000464301.1:n.-43-1731T=