Canonical Allele Identifier: CA8720495
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs763963470

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228067A>T , CM000679.2:g.66228067A>T GRCh38
NC_000017.10:g.64224185A>T , CM000679.1:g.64224185A>T GRCh37
NC_000017.9:g.61654647A>T NCBI36
NG_012045.1:g.6372T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.194T>A MANE Select ENSP00000205948.6:p.Ile65Asn
ENST00000205948.10:c.194T>A ENSP00000205948.6:p.Ile65Asn
ENST00000577982.1:c.194T>A ENSP00000464301.1:p.Ile65Asn
ENST00000581797.5:c.14T>A ENSP00000463553.1:p.Ile5Asn
NM_000042.2:c.194T>A NP_000033.2:p.Ile65Asn
NM_000042.3:c.194T>A MANE Select NP_000033.2:p.Ile65Asn