Canonical Allele Identifier: CA2746056638

Gene: H2BC21

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149885118dup , CM000663.2:g.149885118dup	GRCh38
NC_000001.10:g.149856668dup , CM000663.1:g.149856668dup	GRCh37
NC_000001.9:g.148123292dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369155.4:c.*1145dup MANE Select	ENSP00000358151.2:n.*1145dup
ENST00000369155.3:c.*1145dup	ENSP00000358151.2:n.*1145dup
ENST00000369160.3:c.377+1149dup	ENSP00000375736.2:n.377+1149dup
NM_003528.2:c.*1145dup	NP_003519.1:n.*1145dup
NM_003528.3:c.*1145dup MANE Select	NP_003519.1:n.*1145dup