Canonical Allele Identifier: CA400801842
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073352673

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66214473T>C , CM000679.2:g.66214473T>C GRCh38
NC_000017.10:g.64210591T>C , CM000679.1:g.64210591T>C GRCh37
NC_000017.9:g.61641053T>C NCBI36
NG_012045.1:g.19966A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.962A>G MANE Select ENSP00000205948.6:p.Glu321Gly
ENST00000205948.10:c.962A>G ENSP00000205948.6:p.Glu321Gly
ENST00000585162.1:c.258-2285A>G
NM_000042.2:c.962A>G NP_000033.2:p.Glu321Gly
NM_000042.3:c.962A>G MANE Select NP_000033.2:p.Glu321Gly