Canonical Allele Identifier: CA2478924624

Gene: H2BC21

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149884901T= , CM000663.2:g.149884901T=	GRCh38
NC_000001.10:g.149856451T= , CM000663.1:g.149856451T=	GRCh37
NC_000001.9:g.148123075T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369155.4:c.*1359A= MANE Select	ENSP00000358151.2:n.*1359A=
ENST00000369155.3:c.*1359A=	ENSP00000358151.2:n.*1359A=
ENST00000369160.3:c.377+1363A=	ENSP00000375736.2:n.377+1363A=
NM_003528.2:c.*1359A=	NP_003519.1:n.*1359A=
NM_003528.3:c.*1359A= MANE Select	NP_003519.1:n.*1359A=