Canonical Allele Identifier: CA8720223
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs749413879
ExAC: 17:64210582 T / C
gnomAD v2: 17-64210582-T-C
gnomAD v3: 17-66214464-T-C
gnomAD v4: 17-66214464-T-C
MyVariant Identifiers: chr17:g.64210582T>C (hg19) chr17:g.66214464T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66214464T>C , CM000679.2:g.66214464T>C GRCh38
NC_000017.10:g.64210582T>C , CM000679.1:g.64210582T>C GRCh37
NC_000017.9:g.61641044T>C NCBI36
NG_012045.1:g.19975A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.971A>G MANE Select ENSP00000205948.6:p.Lys324Arg
ENST00000205948.10:c.971A>G ENSP00000205948.6:p.Lys324Arg
ENST00000585162.1:c.258-2276A>G
NM_000042.2:c.971A>G NP_000033.2:p.Lys324Arg
NM_000042.3:c.971A>G MANE Select NP_000033.2:p.Lys324Arg
Search 100 bp 5'
Search 100 bp 3'