Canonical Allele Identifier: CA2478924710

Gene: H2BC21

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149885094_149885096delinsACT , CM000663.2:g.149885094_149885096delinsACT	GRCh38
NC_000001.10:g.149856644_149856646delinsACT , CM000663.1:g.149856644_149856646delinsACT	GRCh37
NC_000001.9:g.148123268_148123270delinsACT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369155.4:c.*1164_*1166delinsAGT MANE Select	ENSP00000358151.2:n.*1164_*1166delinsAGT
ENST00000369155.3:c.*1164_*1166delinsAGT	ENSP00000358151.2:n.*1164_*1166delinsAGT
ENST00000369160.3:c.377+1168_377+1170delinsAGT	ENSP00000375736.2:n.377+1168_377+1170delinsAGT
NM_003528.2:c.*1164_*1166delinsAGT	NP_003519.1:n.*1164_*1166delinsAGT
NM_003528.3:c.*1164_*1166delinsAGT MANE Select	NP_003519.1:n.*1164_*1166delinsAGT