Canonical Allele Identifier: CA2478924698

Gene: H2BC21

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149885061_149885066delinsAAAATC , CM000663.2:g.149885061_149885066delinsAAAATC	GRCh38
NC_000001.10:g.149856611_149856616delinsAAAATC , CM000663.1:g.149856611_149856616delinsAAAATC	GRCh37
NC_000001.9:g.148123235_148123240delinsAAAATC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369155.4:c.*1194_*1199delinsGATTTT MANE Select	ENSP00000358151.2:n.*1194_*1199delinsGATTTT
ENST00000369155.3:c.*1194_*1199delinsGATTTT	ENSP00000358151.2:n.*1194_*1199delinsGATTTT
ENST00000369160.3:c.377+1198_377+1203delinsGATTTT	ENSP00000375736.2:n.377+1198_377+1203delinsGATTTT
NM_003528.2:c.*1194_*1199delinsGATTTT	NP_003519.1:n.*1194_*1199delinsGATTTT
NM_003528.3:c.*1194_*1199delinsGATTTT MANE Select	NP_003519.1:n.*1194_*1199delinsGATTTT