Canonical Allele Identifier: CA985616757
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs148141234
gnomAD v3: 17-66240008-G-C
gnomAD v4: 17-66240008-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240008G>C , CM000679.2:g.66240008G>C GRCh38
NC_000017.10:g.64236126G>C , CM000679.1:g.64236126G>C GRCh37
NC_000017.9:g.61666588G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10586C>G ENSP00000464301.1:n.-43-10586C>G
Search 100 bp 5'
Search 100 bp 3'