Canonical Allele Identifier: CA136260234

Linked Data

dbSNP Id: rs35915781

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107078dup , CM000668.2:g.26107078dup GRCh38
NC_000006.11:g.26107306dup , CM000668.1:g.26107306dup GRCh37
NC_000006.10:g.26215285dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16043dup (H2BC4) ENSP00000516775.1:n.391-16043dup
ENST00000629531.1:c.132+16696dup (H2BC3) ENSP00000486472.1:n.132+16696dup