ClinGen Allele Registry
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Canonical Allele Identifier:
CA12184963
Gene: H2AC9P
HGNC
NCBI
Linked Data
dbSNP Id:
rs10946808
gnomAD v2:
6-26233387-A-G
gnomAD v3:
6-26233159-A-G
gnomAD v4:
6-26233159-A-G
MyVariant Identifiers:
chr6:g.26233387A>G (hg19)
chr6:g.26233159A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.26233159A>G , CM000668.2:g.26233159A>G
GRCh38
NC_000006.11:g.26233387A>G , CM000668.1:g.26233387A>G
GRCh37
NC_000006.10:g.26341366A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid change
ENST00000403259.1:n.38A>G
Search 100 bp 5'
Search 100 bp 3'