Canonical Allele Identifier: CA917700714

Linked Data

dbSNP Id: rs1561950481

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107255_26107256del , CM000668.2:g.26107255_26107256del GRCh38
NC_000006.11:g.26107483_26107484del , CM000668.1:g.26107483_26107484del GRCh37
NC_000006.10:g.26215462_26215463del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000707188.1:c.391-16221_391-16220del (H2BC4) ENSP00000516775.1:n.391-16221_391-16220del
ENST00000629531.1:c.132+16518_132+16519del (H2BC3) ENSP00000486472.1:n.132+16518_132+16519del