Canonical Allele Identifier: CA626914127
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1479650926
gnomAD v2: 17-64235769-A-C
gnomAD v3: 17-66239651-A-C
gnomAD v4: 17-66239651-A-C
MyVariant Identifiers: chr17:g.64235769A>C (hg19) chr17:g.66239651A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239651A>C , CM000679.2:g.66239651A>C GRCh38
NC_000017.10:g.64235769A>C , CM000679.1:g.64235769A>C GRCh37
NC_000017.9:g.61666231A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10229T>G ENSP00000464301.1:n.-43-10229T>G
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