Canonical Allele Identifier: CA8720224
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs758249565
ExAC: 17:64210587 G / A
gnomAD v2: 17-64210587-G-A
gnomAD v3: 17-66214469-G-A
gnomAD v4: 17-66214469-G-A
MyVariant Identifiers: chr17:g.64210587G>A (hg19) chr17:g.66214469G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66214469G>A , CM000679.2:g.66214469G>A GRCh38
NC_000017.10:g.64210587G>A , CM000679.1:g.64210587G>A GRCh37
NC_000017.9:g.61641049G>A NCBI36
NG_012045.1:g.19970C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.966C>T MANE Select ENSP00000205948.6:p.Val322=
ENST00000205948.10:c.966C>T ENSP00000205948.6:p.Val322=
ENST00000585162.1:c.258-2281C>T
NM_000042.2:c.966C>T NP_000033.2:p.Val322=
NM_000042.3:c.966C>T MANE Select NP_000033.2:p.Val322=
Search 100 bp 5'
Search 100 bp 3'