Canonical Allele Identifier: CA2647749610
Gene: H2BC21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884713_149884714insGCC , CM000663.2:g.149884713_149884714insGCC GRCh38
NC_000001.10:g.149856263_149856264insGCC , CM000663.1:g.149856263_149856264insGCC GRCh37
NC_000001.9:g.148122887_148122888insGCC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369155.4:c.*1546_*1547insGGC MANE Select ENSP00000358151.2:n.*1546_*1547insGGC
ENST00000369155.3:c.*1546_*1547insGGC ENSP00000358151.2:n.*1546_*1547insGGC
ENST00000369160.3:c.377+1550_377+1551insGGC ENSP00000375736.2:n.377+1550_377+1551insG...
NM_003528.2:c.*1546_*1547insGGC NP_003519.1:n.*1546_*1547insGGC
NM_003528.3:c.*1546_*1547insGGC MANE Select NP_003519.1:n.*1546_*1547insGGC