Canonical Allele Identifier: CA178367092
Gene: GGH HGNC NCBI

Linked Data

dbSNP Id: rs1040637241

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039094_63039098del , CM000670.2:g.63039094_63039098del GRCh38
NC_000008.10:g.63951653_63951657del , CM000670.1:g.63951653_63951657del GRCh37
NC_000008.9:g.64114207_64114211del NCBI36
NG_028126.1:g.4955_4959del

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.311_315del
ENST00000679326.1:c.-329_-325del ENSP00000504262.1:n.-329_-325del
ENST00000260118.6:c.-329_-325del ENSP00000260118.6:n.-329_-325del
XM_011517623.1:c.-329_-325del XP_011515925.1:n.-329_-325del