Canonical Allele Identifier: CA1616901396

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26116790_26116791delinsCT , CM000668.2:g.26116790_26116791delinsCT GRCh38
NC_000006.11:g.26117018_26117019delinsCT , CM000668.1:g.26117018_26117019delinsCT GRCh37
NC_000006.10:g.26224997_26224998delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.390+6724_390+6725delinsAG (H2BC4) ENSP00000516775.1:n.390+6724_390+6725delinsAG
ENST00000314332.5:c.*10-1656_*10-1655delinsAG (H2BC4) ENSP00000321744.4:n.*10-1656_*10-1655delinsAG
ENST00000629531.1:c.132+6982_132+6983delinsAG (H2BC3) ENSP00000486472.1:n.132+6982_132+6983delinsAG
NM_001381989.1:c.*10-1656_*10-1655delinsAG (H2BC4) NP_001368918.1:n.*10-1656_*10-1655delinsAG