Canonical Allele Identifier: CA293118526
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs769462036

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228074T>G , CM000679.2:g.66228074T>G GRCh38
NC_000017.10:g.64224192T>G , CM000679.1:g.64224192T>G GRCh37
NC_000017.9:g.61654654T>G NCBI36
NG_012045.1:g.6365A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.187A>C MANE Select ENSP00000205948.6:p.Lys63Gln
ENST00000205948.10:c.187A>C ENSP00000205948.6:p.Lys63Gln
ENST00000577982.1:c.187A>C ENSP00000464301.1:p.Lys63Gln
ENST00000581797.5:c.7A>C ENSP00000463553.1:p.Lys3Gln
NM_000042.2:c.187A>C NP_000033.2:p.Lys63Gln
NM_000042.3:c.187A>C MANE Select NP_000033.2:p.Lys63Gln