Canonical Allele Identifier: CA2647749608
Gene: H2BC21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884703_149884707del , CM000663.2:g.149884703_149884707del GRCh38
NC_000001.10:g.149856253_149856257del , CM000663.1:g.149856253_149856257del GRCh37
NC_000001.9:g.148122877_148122881del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369155.4:c.*1553_*1557del MANE Select ENSP00000358151.2:n.*1553_*1557del
ENST00000369155.3:c.*1553_*1557del ENSP00000358151.2:n.*1553_*1557del
ENST00000369160.3:c.377+1557_377+1561del ENSP00000375736.2:n.377+1557_377+1561del
NM_003528.2:c.*1553_*1557del NP_003519.1:n.*1553_*1557del
NM_003528.3:c.*1553_*1557del MANE Select NP_003519.1:n.*1553_*1557del