Canonical Allele Identifier: CA2478924560
Gene: H2BC21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884727T= , CM000663.2:g.149884727T= GRCh38
NC_000001.10:g.149856277T= , CM000663.1:g.149856277T= GRCh37
NC_000001.9:g.148122901T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369155.4:c.*1533A= MANE Select ENSP00000358151.2:n.*1533A=
ENST00000369155.3:c.*1533A= ENSP00000358151.2:n.*1533A=
ENST00000369160.3:c.377+1537A= ENSP00000375736.2:n.377+1537A=
NM_003528.2:c.*1533A= NP_003519.1:n.*1533A=
NM_003528.3:c.*1533A= MANE Select NP_003519.1:n.*1533A=