Canonical Allele Identifier: CA1788923570
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039031G= , CM000670.2:g.63039031G= GRCh38
NC_000008.10:g.63951590G= , CM000670.1:g.63951590G= GRCh37
NC_000008.9:g.64114144G= NCBI36
NG_028126.1:g.5021C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.377C=
ENST00000679326.1:c.-263C= ENSP00000504262.1:n.-263C=
ENST00000260118.6:c.-263C= ENSP00000260118.6:n.-263C=
NM_003878.2:c.-263C= NP_003869.1:n.-263C=
XM_011517623.1:c.-263C= XP_011515925.1:n.-263C=