Canonical Allele Identifier: CA2478924757
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs2092290022
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149885252_149885254del , CM000663.2:g.149885252_149885254del GRCh38
NC_000001.10:g.149856802_149856804del , CM000663.1:g.149856802_149856804del GRCh37
NC_000001.9:g.148123426_148123428del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1008_*1010del MANE Select ENSP00000358151.2:n.*1008_*1010del
ENST00000369155.3:c.*1008_*1010del ENSP00000358151.2:n.*1008_*1010del
ENST00000369160.3:c.377+1012_377+1014del ENSP00000375736.2:n.377+1012_377+1014del
NM_003528.2:c.*1008_*1010del NP_003519.1:n.*1008_*1010del
NM_003528.3:c.*1008_*1010del MANE Select NP_003519.1:n.*1008_*1010del
Search 100 bp 5'
Search 100 bp 3'