Canonical Allele Identifier: CA3693814
Gene: HCG9 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.29975290G>A
GRCh37 chr6:g.29943067G>A
gnomAD v2:
6:29943067 G / A
gnomAD v3:
6:29975290 G / A
gnomAD v4:
chr6-29975290-G-A
Joint Max Group AF 0.31227721 (EAS)
Genomes Max Group AF 0.29863262 (EAS)
Exomes Max Group AF 0.3207426 (AMR)
dbSNP:
6904029
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29975290G>A , CM000668.2:g.29975290G>A GRCh38
NC_000006.11:g.29943067G>A , CM000668.1:g.29943067G>A GRCh37
NC_000006.10:g.30051046G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028032.1:n.176G>A
Search 100 bp 5'
Search 100 bp 3'