Canonical Allele Identifier: CA2593925718

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26116769_26116770del , CM000668.2:g.26116769_26116770del GRCh38
NC_000006.11:g.26116997_26116998del , CM000668.1:g.26116997_26116998del GRCh37
NC_000006.10:g.26224976_26224977del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.390+6749_390+6750del (H2BC4) ENSP00000516775.1:n.390+6749_390+6750del
ENST00000314332.5:c.*10-1631_*10-1630del (H2BC4) ENSP00000321744.4:n.*10-1631_*10-1630del
ENST00000629531.1:c.132+7007_132+7008del (H2BC3) ENSP00000486472.1:n.132+7007_132+7008del
NM_001381989.1:c.*10-1631_*10-1630del (H2BC4) NP_001368918.1:n.*10-1631_*10-1630del