Canonical Allele Identifier: CA2647749612
Gene: H2BC21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884718_149884720del , CM000663.2:g.149884718_149884720del GRCh38
NC_000001.10:g.149856268_149856270del , CM000663.1:g.149856268_149856270del GRCh37
NC_000001.9:g.148122892_148122894del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369155.4:c.*1541_*1543del MANE Select ENSP00000358151.2:n.*1541_*1543del
ENST00000369155.3:c.*1541_*1543del ENSP00000358151.2:n.*1541_*1543del
ENST00000369160.3:c.377+1545_377+1547del ENSP00000375736.2:n.377+1545_377+1547del
NM_003528.2:c.*1541_*1543del NP_003519.1:n.*1541_*1543del
NM_003528.3:c.*1541_*1543del MANE Select NP_003519.1:n.*1541_*1543del