Canonical Allele Identifier: CA985610647
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073449414

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66227953G>T , CM000679.2:g.66227953G>T GRCh38
NC_000017.10:g.64224071G>T , CM000679.1:g.64224071G>T GRCh37
NC_000017.9:g.61654533G>T NCBI36
NG_012045.1:g.6486C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.241+67C>A MANE Select ENSP00000205948.6:n.241+67C>A
ENST00000205948.10:c.241+67C>A ENSP00000205948.6:n.241+67C>A
ENST00000577982.1:c.241+67C>A ENSP00000464301.1:n.241+67C>A
ENST00000581797.5:c.61+67C>A ENSP00000463553.1:n.61+67C>A
NM_000042.2:c.241+67C>A NP_000033.2:n.241+67C>A
NM_000042.3:c.241+67C>A MANE Select NP_000033.2:n.241+67C>A