Canonical Allele Identifier: CA2687440128
Gene: GGH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038908_63038909del , CM000670.2:g.63038908_63038909del GRCh38
NC_000008.10:g.63951467_63951468del , CM000670.1:g.63951467_63951468del GRCh37
NC_000008.9:g.64114021_64114022del NCBI36
NG_028126.1:g.5143_5144del

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.499_500del
ENST00000679326.1:c.-141_-140del ENSP00000504262.1:n.-141_-140del
ENST00000260118.6:c.-141_-140del ENSP00000260118.6:n.-141_-140del
NM_003878.2:c.-141_-140del NP_003869.1:n.-141_-140del
XM_011517623.1:c.-141_-140del XP_011515925.1:n.-141_-140del