Canonical Allele Identifier: CA2478924697

Gene: H2BC21

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149885056_149885057delinsCA , CM000663.2:g.149885056_149885057delinsCA	GRCh38
NC_000001.10:g.149856606_149856607delinsCA , CM000663.1:g.149856606_149856607delinsCA	GRCh37
NC_000001.9:g.148123230_148123231delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369155.4:c.*1203_*1204delinsTG MANE Select	ENSP00000358151.2:n.*1203_*1204delinsTG
ENST00000369155.3:c.*1203_*1204delinsTG	ENSP00000358151.2:n.*1203_*1204delinsTG
ENST00000369160.3:c.377+1207_377+1208delinsTG	ENSP00000375736.2:n.377+1207_377+1208delinsTG
NM_003528.2:c.*1203_*1204delinsTG	NP_003519.1:n.*1203_*1204delinsTG
NM_003528.3:c.*1203_*1204delinsTG MANE Select	NP_003519.1:n.*1203_*1204delinsTG