Canonical Allele Identifier: CA823452937

Linked Data

dbSNP Id: rs1453860656

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107154_26107156dup , CM000668.2:g.26107154_26107156dup GRCh38
NC_000006.11:g.26107382_26107384dup , CM000668.1:g.26107382_26107384dup GRCh37
NC_000006.10:g.26215361_26215363dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16121_391-16119dup (H2BC4) ENSP00000516775.1:n.391-16121_391-16119du...
ENST00000629531.1:c.132+16618_132+16620dup (H2BC3) ENSP00000486472.1:n.132+16618_132+16620du...