ClinGen Allele Registry
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Canonical Allele Identifier:
CA136260702
Gene: H2AC9P
HGNC
NCBI
Linked Data
dbSNP Id:
rs984548367
gnomAD v3:
6-26233179-T-A
gnomAD v4:
6-26233179-T-A
MyVariant Identifiers:
chr6:g.26233407T>A (hg19)
chr6:g.26233179T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.26233179T>A , CM000668.2:g.26233179T>A
GRCh38
NC_000006.11:g.26233407T>A , CM000668.1:g.26233407T>A
GRCh37
NC_000006.10:g.26341386T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000403259.1:n.58T>A
Search 100 bp 5'
Search 100 bp 3'