Canonical Allele Identifier: CA8720515
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs666

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228153C>T , CM000679.2:g.66228153C>T GRCh38
NC_000017.10:g.64224271C>T , CM000679.1:g.64224271C>T GRCh37
NC_000017.9:g.61654733C>T NCBI36
NG_012045.1:g.6286G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.108G>A MANE Select ENSP00000205948.6:p.Pro36=
ENST00000205948.10:c.108G>A ENSP00000205948.6:p.Pro36=
ENST00000577982.1:c.108G>A ENSP00000464301.1:p.Pro36=
ENST00000581797.5:c.-73G>A ENSP00000463553.1:p.=
NM_000042.2:c.108G>A NP_000033.2:p.Pro36=
NM_000042.3:c.108G>A MANE Select NP_000033.2:p.Pro36=