Canonical Allele Identifier: CA1788923588
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039070A= , CM000670.2:g.63039070A= GRCh38
NC_000008.10:g.63951629A= , CM000670.1:g.63951629A= GRCh37
NC_000008.9:g.64114183A= NCBI36
NG_028126.1:g.4982T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.338T=
ENST00000679326.1:c.-302T= ENSP00000504262.1:n.-302T=
ENST00000260118.6:c.-302T= ENSP00000260118.6:n.-302T=
XM_011517623.1:c.-302T= XP_011515925.1:n.-302T=