Canonical Allele Identifier: CA400801827
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64210585G>C (hg19) chr17:g.66214467G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66214467G>C , CM000679.2:g.66214467G>C GRCh38
NC_000017.10:g.64210585G>C , CM000679.1:g.64210585G>C GRCh37
NC_000017.9:g.61641047G>C NCBI36
NG_012045.1:g.19972C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.968C>G MANE Select ENSP00000205948.6:p.Pro323Arg
ENST00000205948.10:c.968C>G ENSP00000205948.6:p.Pro323Arg
ENST00000585162.1:c.258-2279C>G
NM_000042.2:c.968C>G NP_000033.2:p.Pro323Arg
NM_000042.3:c.968C>G MANE Select NP_000033.2:p.Pro323Arg
Search 100 bp 5'
Search 100 bp 3'