Canonical Allele Identifier: CA8720518
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs566373863
ExAC: 17:64224285 A / C
gnomAD v2: 17-64224285-A-C
gnomAD v3: 17-66228167-A-C
gnomAD v4: 17-66228167-A-C
MyVariant Identifiers: chr17:g.64224285A>C (hg19) chr17:g.66228167A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228167A>C , CM000679.2:g.66228167A>C GRCh38
NC_000017.10:g.64224285A>C , CM000679.1:g.64224285A>C GRCh37
NC_000017.9:g.61654747A>C NCBI36
NG_012045.1:g.6272T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.94T>G MANE Select ENSP00000205948.6:p.Ser32Ala
ENST00000205948.10:c.94T>G ENSP00000205948.6:p.Ser32Ala
ENST00000577982.1:c.94T>G ENSP00000464301.1:p.Ser32Ala
ENST00000581797.5:c.-87T>G ENSP00000463553.1:n.-87T>G
NM_000042.2:c.94T>G NP_000033.2:p.Ser32Ala
NM_000042.3:c.94T>G MANE Select NP_000033.2:p.Ser32Ala
Search 100 bp 5'
Search 100 bp 3'