Canonical Allele Identifier: CA2478924556
Gene: H2BC21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884715_149884717delinsCTA , CM000663.2:g.149884715_149884717delinsCTA GRCh38
NC_000001.10:g.149856265_149856267delinsCTA , CM000663.1:g.149856265_149856267delinsCTA GRCh37
NC_000001.9:g.148122889_148122891delinsCTA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369155.4:c.*1543_*1545delinsTAG MANE Select ENSP00000358151.2:n.*1543_*1545delinsTAG
ENST00000369155.3:c.*1543_*1545delinsTAG ENSP00000358151.2:n.*1543_*1545delinsTAG
ENST00000369160.3:c.377+1547_377+1549delinsTAG ENSP00000375736.2:n.377+1547_377+1549deli...
NM_003528.2:c.*1543_*1545delinsTAG NP_003519.1:n.*1543_*1545delinsTAG
NM_003528.3:c.*1543_*1545delinsTAG MANE Select NP_003519.1:n.*1543_*1545delinsTAG