Canonical Allele Identifier: CA1616901403

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26116809T= , CM000668.2:g.26116809T= GRCh38
NC_000006.11:g.26117037T= , CM000668.1:g.26117037T= GRCh37
NC_000006.10:g.26225016T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.390+6706A= (H2BC4) ENSP00000516775.1:n.390+6706A=
ENST00000314332.5:c.*10-1674A= (H2BC4) ENSP00000321744.4:n.*10-1674A=
ENST00000629531.1:c.132+6964A= (H2BC3) ENSP00000486472.1:n.132+6964A=
NM_001381989.1:c.*10-1674A= (H2BC4) NP_001368918.1:n.*10-1674A=