Canonical Allele Identifier: CA293118525
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs747763235

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228073T>C , CM000679.2:g.66228073T>C GRCh38
NC_000017.10:g.64224191T>C , CM000679.1:g.64224191T>C GRCh37
NC_000017.9:g.61654653T>C NCBI36
NG_012045.1:g.6366A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.188A>G MANE Select ENSP00000205948.6:p.Lys63Arg
ENST00000205948.10:c.188A>G ENSP00000205948.6:p.Lys63Arg
ENST00000577982.1:c.188A>G ENSP00000464301.1:p.Lys63Arg
ENST00000581797.5:c.8A>G ENSP00000463553.1:p.Lys3Arg
NM_000042.2:c.188A>G NP_000033.2:p.Lys63Arg
NM_000042.3:c.188A>G MANE Select NP_000033.2:p.Lys63Arg