Canonical Allele Identifier: CA2478924756

Gene: H2BC21

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149885249_149885252delinsATAT , CM000663.2:g.149885249_149885252delinsATAT	GRCh38
NC_000001.10:g.149856799_149856802delinsATAT , CM000663.1:g.149856799_149856802delinsATAT	GRCh37
NC_000001.9:g.148123423_148123426delinsATAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369155.4:c.*1008_*1011delinsATAT MANE Select	ENSP00000358151.2:n.*1008_*1011delinsATAT
ENST00000369155.3:c.*1008_*1011delinsATAT	ENSP00000358151.2:n.*1008_*1011delinsATAT
ENST00000369160.3:c.377+1012_377+1015delinsATAT	ENSP00000375736.2:n.377+1012_377+1015delinsATAT
NM_003528.2:c.*1008_*1011delinsATAT	NP_003519.1:n.*1008_*1011delinsATAT
NM_003528.3:c.*1008_*1011delinsATAT MANE Select	NP_003519.1:n.*1008_*1011delinsATAT