Canonical Allele Identifier: CA14498517
Gene: APOH HGNC NCBI
dbSNP:
10048158
gnomAD v2:
17:64236318 T / C
gnomAD v3:
17:66240200 T / C
gnomAD v4:
chr17-66240200-T-C
Joint Max Group AF 0.90156509 (EAS)
Genomes Max Group AF 0.90156509 (EAS)
MyVariant.info:
GRCh38 chr17:g.66240200T>C
GRCh37 chr17:g.64236318T>C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240200T>C , CM000679.2:g.66240200T>C GRCh38
NC_000017.10:g.64236318T>C , CM000679.1:g.64236318T>C GRCh37
NC_000017.9:g.61666780T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10778A>G ENSP00000464301.1:n.-43-10778A>G
Search 100 bp 5'
Search 100 bp 3'