Canonical Allele Identifier: CA2478924740

Gene: H2BC21

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149885193_149885197delinsTCATC , CM000663.2:g.149885193_149885197delinsTCATC	GRCh38
NC_000001.10:g.149856743_149856747delinsTCATC , CM000663.1:g.149856743_149856747delinsTCATC	GRCh37
NC_000001.9:g.148123367_148123371delinsTCATC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369155.4:c.*1063_*1067delinsGATGA MANE Select	ENSP00000358151.2:n.*1063_*1067delinsGATGA
ENST00000369155.3:c.*1063_*1067delinsGATGA	ENSP00000358151.2:n.*1063_*1067delinsGATGA
ENST00000369160.3:c.377+1067_377+1071delinsGATGA	ENSP00000375736.2:n.377+1067_377+1071delinsGATGA
NM_003528.2:c.*1063_*1067delinsGATGA	NP_003519.1:n.*1063_*1067delinsGATGA
NM_003528.3:c.*1063_*1067delinsGATGA MANE Select	NP_003519.1:n.*1063_*1067delinsGATGA