Canonical Allele Identifier: CA400683805
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228095C>G , CM000679.2:g.66228095C>G GRCh38
NC_000017.10:g.64224213C>G , CM000679.1:g.64224213C>G GRCh37
NC_000017.9:g.61654675C>G NCBI36
NG_012045.1:g.6344G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.166G>C MANE Select ENSP00000205948.6:p.Val56Leu
ENST00000205948.10:c.166G>C ENSP00000205948.6:p.Val56Leu
ENST00000577982.1:c.166G>C ENSP00000464301.1:p.Val56Leu
ENST00000581797.5:c.-15G>C ENSP00000463553.1:n.-15G>C
NM_000042.2:c.166G>C NP_000033.2:p.Val56Leu
NM_000042.3:c.166G>C MANE Select NP_000033.2:p.Val56Leu