Canonical Allele Identifier: CA1616896858

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107263_26107267delinsTCTGG , CM000668.2:g.26107263_26107267delinsTCTGG GRCh38
NC_000006.11:g.26107491_26107495delinsTCTGG , CM000668.1:g.26107491_26107495delinsTCTGG GRCh37
NC_000006.10:g.26215470_26215474delinsTCTGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16233_391-16229delinsCCAGA (H2BC4) ENSP00000516775.1:n.391-16233_391-16229delinsCCAGA
ENST00000629531.1:c.132+16506_132+16510delinsCCAGA (H2BC3) ENSP00000486472.1:n.132+16506_132+16510delinsCCAGA