Canonical Allele Identifier: CA526023841
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1479695393

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884758del , CM000663.2:g.149884758del GRCh38
NC_000001.10:g.149856308del , CM000663.1:g.149856308del GRCh37
NC_000001.9:g.148122932del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369155.4:c.*1502del MANE Select ENSP00000358151.2:n.*1502del
ENST00000369155.3:c.*1502del ENSP00000358151.2:n.*1502del
ENST00000369160.3:c.377+1506del ENSP00000375736.2:n.377+1506del
NM_003528.2:c.*1502del NP_003519.1:n.*1502del
NM_003528.3:c.*1502del MANE Select NP_003519.1:n.*1502del