Canonical Allele Identifier: CA2271193190
Gene: APOH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66231202G= , CM000679.2:g.66231202G= GRCh38
NC_000017.10:g.64227320G= , CM000679.1:g.64227320G= GRCh37
NC_000017.9:g.61657782G= NCBI36
NG_012045.1:g.3237C=

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-1780C= ENSP00000464301.1:n.-43-1780C=