Canonical Allele Identifier: CA823452927

Linked Data

dbSNP Id: rs1317677566

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107135dup , CM000668.2:g.26107135dup GRCh38
NC_000006.11:g.26107363dup , CM000668.1:g.26107363dup GRCh37
NC_000006.10:g.26215342dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16101dup (H2BC4) ENSP00000516775.1:n.391-16101dup
ENST00000629531.1:c.132+16638dup (H2BC3) ENSP00000486472.1:n.132+16638dup