Canonical Allele Identifier: CA917700712

Linked Data

dbSNP Id: rs1581684148

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107213_26107215dup , CM000668.2:g.26107213_26107215dup GRCh38
NC_000006.11:g.26107441_26107443dup , CM000668.1:g.26107441_26107443dup GRCh37
NC_000006.10:g.26215420_26215422dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16181_391-16179dup (H2BC4) ENSP00000516775.1:n.391-16181_391-16179dup
ENST00000629531.1:c.132+16558_132+16560dup (H2BC3) ENSP00000486472.1:n.132+16558_132+16560dup