Canonical Allele Identifier: CA400801822
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64210582T>A (hg19) chr17:g.66214464T>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.971A>T MANE Select ENSP00000205948.6:p.Lys324Ile
ENST00000205948.10:c.971A>T ENSP00000205948.6:p.Lys324Ile
ENST00000585162.1:c.258-2276A>T
NM_000042.2:c.971A>T NP_000033.2:p.Lys324Ile
NM_000042.3:c.971A>T MANE Select NP_000033.2:p.Lys324Ile
Search 100 bp 5'
Search 100 bp 3'