Canonical Allele Identifier: CA2478924728
Gene: H2BC21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149885140T= , CM000663.2:g.149885140T= GRCh38
NC_000001.10:g.149856690T= , CM000663.1:g.149856690T= GRCh37
NC_000001.9:g.148123314T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1120A= MANE Select ENSP00000358151.2:n.*1120A=
ENST00000369155.3:c.*1120A= ENSP00000358151.2:n.*1120A=
ENST00000369160.3:c.377+1124A= ENSP00000375736.2:n.377+1124A=
NM_003528.2:c.*1120A= NP_003519.1:n.*1120A=
NM_003528.3:c.*1120A= MANE Select NP_003519.1:n.*1120A=