Canonical Allele Identifier: CA2478924428
Gene: H2BC21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884397T= , CM000663.2:g.149884397T= GRCh38
NC_000001.10:g.149855947T= , CM000663.1:g.149855947T= GRCh37
NC_000001.9:g.148122571T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1867A= ENSP00000375736.2:n.377+1867A=