Canonical Allele Identifier: CA916306491
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs1571465310
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884929_149884936del , CM000663.2:g.149884929_149884936del GRCh38
NC_000001.10:g.149856479_149856486del , CM000663.1:g.149856479_149856486del GRCh37
NC_000001.9:g.148123103_148123110del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1324_*1331del MANE Select ENSP00000358151.2:n.*1324_*1331del
ENST00000369155.3:c.*1324_*1331del ENSP00000358151.2:n.*1324_*1331del
ENST00000369160.3:c.377+1328_377+1335del ENSP00000375736.2:n.377+1328_377+1335del
NM_003528.2:c.*1324_*1331del NP_003519.1:n.*1324_*1331del
NM_003528.3:c.*1324_*1331del MANE Select NP_003519.1:n.*1324_*1331del
Search 100 bp 5'
Search 100 bp 3'