Canonical Allele Identifier: CA400801840
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64210590T>G (hg19) chr17:g.66214472T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66214472T>G , CM000679.2:g.66214472T>G GRCh38
NC_000017.10:g.64210590T>G , CM000679.1:g.64210590T>G GRCh37
NC_000017.9:g.61641052T>G NCBI36
NG_012045.1:g.19967A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.963A>C MANE Select ENSP00000205948.6:p.Glu321Asp
ENST00000205948.10:c.963A>C ENSP00000205948.6:p.Glu321Asp
ENST00000585162.1:c.258-2284A>C
NM_000042.2:c.963A>C NP_000033.2:p.Glu321Asp
NM_000042.3:c.963A>C MANE Select NP_000033.2:p.Glu321Asp
Search 100 bp 5'
Search 100 bp 3'