Canonical Allele Identifier: CA2576362537
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66227954C>T , CM000679.2:g.66227954C>T GRCh38
NC_000017.10:g.64224072C>T , CM000679.1:g.64224072C>T GRCh37
NC_000017.9:g.61654534C>T NCBI36
NG_012045.1:g.6485G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.241+66G>A MANE Select ENSP00000205948.6:n.241+66G>A
ENST00000205948.10:c.241+66G>A ENSP00000205948.6:n.241+66G>A
ENST00000577982.1:c.241+66G>A ENSP00000464301.1:n.241+66G>A
ENST00000581797.5:c.61+66G>A ENSP00000463553.1:n.61+66G>A
NM_000042.2:c.241+66G>A NP_000033.2:n.241+66G>A
NM_000042.3:c.241+66G>A MANE Select NP_000033.2:n.241+66G>A