Canonical Allele Identifier: CA1788923622
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039123A= , CM000670.2:g.63039123A= GRCh38
NC_000008.10:g.63951682A= , CM000670.1:g.63951682A= GRCh37
NC_000008.9:g.64114236A= NCBI36
NG_028126.1:g.4929T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.285T=
ENST00000679326.1:c.-355T= ENSP00000504262.1:n.-355T=
ENST00000260118.6:c.-355T= ENSP00000260118.6:n.-355T=
XM_011517623.1:c.-355T= XP_011515925.1:n.-355T=