Canonical Allele Identifier: CA400683748
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228064C>G , CM000679.2:g.66228064C>G GRCh38
NC_000017.10:g.64224182C>G , CM000679.1:g.64224182C>G GRCh37
NC_000017.9:g.61654644C>G NCBI36
NG_012045.1:g.6375G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.197G>C MANE Select ENSP00000205948.6:p.Cys66Ser
ENST00000205948.10:c.197G>C ENSP00000205948.6:p.Cys66Ser
ENST00000577982.1:c.197G>C ENSP00000464301.1:p.Cys66Ser
ENST00000581797.5:c.17G>C ENSP00000463553.1:p.Cys6Ser
NM_000042.2:c.197G>C NP_000033.2:p.Cys66Ser
NM_000042.3:c.197G>C MANE Select NP_000033.2:p.Cys66Ser