ClinGen Allele Registry
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Canonical Allele Identifier:
CA1139816508
Gene: H2BC18
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.149756186C= , CM000663.2:g.149756186C=
GRCh38
NC_000001.10:g.149727736C= , CM000663.1:g.149727736C=
GRCh37
Transcript Alleles
HGVS
Amino-acid Change
XM_006711337.2:c.*87G=
XP_006711400.1:n.*87G=
Search 100 bp 5'
Search 100 bp 3'