ClinGen Allele Registry
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Canonical Allele Identifier:
CA1616962345
Gene: H2AC9P
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.26233172G= , CM000668.2:g.26233172G=
GRCh38
NC_000006.11:g.26233400G= , CM000668.1:g.26233400G=
GRCh37
NC_000006.10:g.26341379G=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000403259.1:n.51G=
Search 100 bp 5'
Search 100 bp 3'