Canonical Allele Identifier: CA2639419280
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66227949G>T , CM000679.2:g.66227949G>T GRCh38
NC_000017.10:g.64224067G>T , CM000679.1:g.64224067G>T GRCh37
NC_000017.9:g.61654529G>T NCBI36
NG_012045.1:g.6490C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.241+71C>A MANE Select ENSP00000205948.6:n.241+71C>A
ENST00000205948.10:c.241+71C>A ENSP00000205948.6:n.241+71C>A
ENST00000577982.1:c.241+71C>A ENSP00000464301.1:n.241+71C>A
ENST00000581797.5:c.61+71C>A ENSP00000463553.1:n.61+71C>A
NM_000042.2:c.241+71C>A NP_000033.2:n.241+71C>A
NM_000042.3:c.241+71C>A MANE Select NP_000033.2:n.241+71C>A