Canonical Allele Identifier: CA293118530
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1025512314

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.166G>A MANE Select ENSP00000205948.6:p.Val56Met
ENST00000205948.10:c.166G>A ENSP00000205948.6:p.Val56Met
ENST00000577982.1:c.166G>A ENSP00000464301.1:p.Val56Met
ENST00000581797.5:c.-15G>A ENSP00000463553.1:n.-15G>A
NM_000042.2:c.166G>A NP_000033.2:p.Val56Met
NM_000042.3:c.166G>A MANE Select NP_000033.2:p.Val56Met