Canonical Allele Identifier: CA2478924557
Gene: H2BC21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884721T= , CM000663.2:g.149884721T= GRCh38
NC_000001.10:g.149856271T= , CM000663.1:g.149856271T= GRCh37
NC_000001.9:g.148122895T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369155.4:c.*1539A= MANE Select ENSP00000358151.2:n.*1539A=
ENST00000369155.3:c.*1539A= ENSP00000358151.2:n.*1539A=
ENST00000369160.3:c.377+1543A= ENSP00000375736.2:n.377+1543A=
NM_003528.2:c.*1539A= NP_003519.1:n.*1539A=
NM_003528.3:c.*1539A= MANE Select NP_003519.1:n.*1539A=