Canonical Allele Identifier: CA2687440398
Gene: GGH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039124dup , CM000670.2:g.63039124dup GRCh38
NC_000008.10:g.63951683dup , CM000670.1:g.63951683dup GRCh37
NC_000008.9:g.64114237dup NCBI36
NG_028126.1:g.4928dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.284dup
ENST00000679326.1:c.-356dup ENSP00000504262.1:n.-356dup
ENST00000260118.6:c.-356dup ENSP00000260118.6:n.-356dup
XM_011517623.1:c.-356dup XP_011515925.1:n.-356dup