Canonical Allele Identifier: CA400683905
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228140A>C , CM000679.2:g.66228140A>C GRCh38
NC_000017.10:g.64224258A>C , CM000679.1:g.64224258A>C GRCh37
NC_000017.9:g.61654720A>C NCBI36
NG_012045.1:g.6299T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.121T>G MANE Select ENSP00000205948.6:p.Tyr41Asp
ENST00000205948.10:c.121T>G ENSP00000205948.6:p.Tyr41Asp
ENST00000577982.1:c.121T>G ENSP00000464301.1:p.Tyr41Asp
ENST00000581797.5:c.-60T>G ENSP00000463553.1:n.-60T>G
NM_000042.2:c.121T>G NP_000033.2:p.Tyr41Asp
NM_000042.3:c.121T>G MANE Select NP_000033.2:p.Tyr41Asp