Canonical Allele Identifier: CA889168802

Gene: H2BC21

Linked Data

• dbSNP Id: rs1264535739
• MyVariant Identifiers: chr1:g.149885106_149885108del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149885106_149885108del , CM000663.2:g.149885106_149885108del	GRCh38
NC_000001.10:g.149856656_149856658del , CM000663.1:g.149856656_149856658del	GRCh37
NC_000001.9:g.148123280_148123282del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369155.4:c.*1152_*1154del MANE Select	ENSP00000358151.2:n.*1152_*1154del
ENST00000369155.3:c.*1152_*1154del	ENSP00000358151.2:n.*1152_*1154del
ENST00000369160.3:c.377+1156_377+1158del	ENSP00000375736.2:n.377+1156_377+1158del
NM_003528.2:c.*1152_*1154del	NP_003519.1:n.*1152_*1154del
NM_003528.3:c.*1152_*1154del MANE Select	NP_003519.1:n.*1152_*1154del