Canonical Allele Identifier: CA2687440107
Gene: GGH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038899dup , CM000670.2:g.63038899dup GRCh38
NC_000008.10:g.63951458dup , CM000670.1:g.63951458dup GRCh37
NC_000008.9:g.64114012dup NCBI36
NG_028126.1:g.5155dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.511dup
ENST00000679326.1:c.-129dup ENSP00000504262.1:n.-129dup
ENST00000260118.6:c.-129dup ENSP00000260118.6:n.-129dup
NM_003878.2:c.-129dup NP_003869.1:n.-129dup
XM_011517623.1:c.-129dup XP_011515925.1:n.-129dup