Canonical Allele Identifier: CA400683885
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073451118

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228131C>T , CM000679.2:g.66228131C>T GRCh38
NC_000017.10:g.64224249C>T , CM000679.1:g.64224249C>T GRCh37
NC_000017.9:g.61654711C>T NCBI36
NG_012045.1:g.6308G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.130G>A MANE Select ENSP00000205948.6:p.Gly44Arg
ENST00000205948.10:c.130G>A ENSP00000205948.6:p.Gly44Arg
ENST00000577982.1:c.130G>A ENSP00000464301.1:p.Gly44Arg
ENST00000581797.5:c.-51G>A ENSP00000463553.1:n.-51G>A
NM_000042.2:c.130G>A NP_000033.2:p.Gly44Arg
NM_000042.3:c.130G>A MANE Select NP_000033.2:p.Gly44Arg