Canonical Allele Identifier: CA1141148260
Gene: H2BC21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884354C= , CM000663.2:g.149884354C= GRCh38
NC_000001.10:g.149855904C= , CM000663.1:g.149855904C= GRCh37
NC_000001.9:g.148122528C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1910G= ENSP00000375736.2:n.377+1910G=