Canonical Allele Identifier: CA2478924741

Gene: H2BC21

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149885195A= , CM000663.2:g.149885195A=	GRCh38
NC_000001.10:g.149856745A= , CM000663.1:g.149856745A=	GRCh37
NC_000001.9:g.148123369A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369155.4:c.*1065T= MANE Select	ENSP00000358151.2:n.*1065T=
ENST00000369155.3:c.*1065T=	ENSP00000358151.2:n.*1065T=
ENST00000369160.3:c.377+1069T=	ENSP00000375736.2:n.377+1069T=
NM_003528.2:c.*1065T=	NP_003519.1:n.*1065T=
NM_003528.3:c.*1065T= MANE Select	NP_003519.1:n.*1065T=