Canonical Allele Identifier: CA136260240

Linked Data

dbSNP Id: rs1047580188

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107103_26107106del , CM000668.2:g.26107103_26107106del GRCh38
NC_000006.11:g.26107331_26107334del , CM000668.1:g.26107331_26107334del GRCh37
NC_000006.10:g.26215310_26215313del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16072_391-16069del (H2BC4) ENSP00000516775.1:n.391-16072_391-16069del
ENST00000629531.1:c.132+16667_132+16670del (H2BC3) ENSP00000486472.1:n.132+16667_132+16670del