Canonical Allele Identifier: CA2478924521
Gene: H2BC21 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884611_149884621delinsTAGCCAAAAAC , CM000663.2:g.149884611_149884621delinsTAGCCAAAAAC GRCh38
NC_000001.10:g.149856161_149856171delinsTAGCCAAAAAC , CM000663.1:g.149856161_149856171delinsTAGCCAAAAAC GRCh37
NC_000001.9:g.148122785_148122795delinsTAGCCAAAAAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369155.4:c.*1639_*1649delinsGTTTTTGGCTA MANE Select ENSP00000358151.2:n.*1639_*1649delinsGTTTTTGGCTA
ENST00000369155.3:c.*1639_*1649delinsGTTTTTGGCTA ENSP00000358151.2:n.*1639_*1649delinsGTTTTTGGCTA
ENST00000369160.3:c.377+1643_377+1653delinsGTTTTTGGCTA ENSP00000375736.2:n.377+1643_377+1653delinsGTTTTTGGCTA
NM_003528.2:c.*1639_*1649delinsGTTTTTGGCTA NP_003519.1:n.*1639_*1649delinsGTTTTTGGCTA
NM_003528.3:c.*1639_*1649delinsGTTTTTGGCTA MANE Select NP_003519.1:n.*1639_*1649delinsGTTTTTGGCTA
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Search 100 bp 3'