Canonical Allele Identifier: CA400683997
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1471958766
gnomAD v4: 17-66228182-C-T
MyVariant Identifiers: chr17:g.64224300C>T (hg19) chr17:g.66228182C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228182C>T , CM000679.2:g.66228182C>T GRCh38
NC_000017.10:g.64224300C>T , CM000679.1:g.64224300C>T GRCh37
NC_000017.9:g.61654762C>T NCBI36
NG_012045.1:g.6257G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.79G>A MANE Select ENSP00000205948.6:p.Asp27Asn
ENST00000205948.10:c.79G>A ENSP00000205948.6:p.Asp27Asn
ENST00000577982.1:c.79G>A ENSP00000464301.1:p.Asp27Asn
ENST00000581797.5:c.-102G>A ENSP00000463553.1:n.-102G>A
NM_000042.2:c.79G>A NP_000033.2:p.Asp27Asn
NM_000042.3:c.79G>A MANE Select NP_000033.2:p.Asp27Asn
Search 100 bp 5'
Search 100 bp 3'