Canonical Allele Identifier: CA2687440192
Gene: GGH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038967_63038973del , CM000670.2:g.63038967_63038973del GRCh38
NC_000008.10:g.63951526_63951532del , CM000670.1:g.63951526_63951532del GRCh37
NC_000008.9:g.64114080_64114086del NCBI36
NG_028126.1:g.5083_5089del

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.439_445del
ENST00000679326.1:c.-201_-195del ENSP00000504262.1:n.-201_-195del
ENST00000260118.6:c.-201_-195del ENSP00000260118.6:n.-201_-195del
NM_003878.2:c.-201_-195del NP_003869.1:n.-201_-195del
XM_011517623.1:c.-201_-195del XP_011515925.1:n.-201_-195del