Canonical Allele Identifier: CA626914122
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1215359444
gnomAD v2: 17-64235721-C-G
gnomAD v3: 17-66239603-C-G
gnomAD v4: 17-66239603-C-G
MyVariant Identifiers: chr17:g.64235721C>G (hg19) chr17:g.66239603C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239603C>G , CM000679.2:g.66239603C>G GRCh38
NC_000017.10:g.64235721C>G , CM000679.1:g.64235721C>G GRCh37
NC_000017.9:g.61666183C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10181G>C ENSP00000464301.1:n.-43-10181G>C
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