Canonical Allele Identifier: CA1788923579
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039042G= , CM000670.2:g.63039042G= GRCh38
NC_000008.10:g.63951601G= , CM000670.1:g.63951601G= GRCh37
NC_000008.9:g.64114155G= NCBI36
NG_028126.1:g.5010C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.366C=
ENST00000679326.1:c.-274C= ENSP00000504262.1:n.-274C=
ENST00000260118.6:c.-274C= ENSP00000260118.6:n.-274C=
NM_003878.2:c.-274C= NP_003869.1:n.-274C=
XM_011517623.1:c.-274C= XP_011515925.1:n.-274C=