ClinGen Allele Registry
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Canonical Allele Identifier:
CA448985541
Gene: H2AC9P
HGNC
NCBI
Linked Data
dbSNP Id:
rs1759684542
MyVariant Identifiers:
chr6:g.26233457T>C (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.26233229T>C , CM000668.2:g.26233229T>C
GRCh38
NC_000006.11:g.26233457T>C , CM000668.1:g.26233457T>C
GRCh37
NC_000006.10:g.26341436T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000403259.1:n.108T>C
Search 100 bp 5'
Search 100 bp 3'