Canonical Allele Identifier: CA2478924558
Gene: H2BC21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884725A= , CM000663.2:g.149884725A= GRCh38
NC_000001.10:g.149856275A= , CM000663.1:g.149856275A= GRCh37
NC_000001.9:g.148122899A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369155.4:c.*1535T= MANE Select ENSP00000358151.2:n.*1535T=
ENST00000369155.3:c.*1535T= ENSP00000358151.2:n.*1535T=
ENST00000369160.3:c.377+1539T= ENSP00000375736.2:n.377+1539T=
NM_003528.2:c.*1535T= NP_003519.1:n.*1535T=
NM_003528.3:c.*1535T= MANE Select NP_003519.1:n.*1535T=