Canonical Allele Identifier: CA1788923551
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039004C= , CM000670.2:g.63039004C= GRCh38
NC_000008.10:g.63951563C= , CM000670.1:g.63951563C= GRCh37
NC_000008.9:g.64114117C= NCBI36
NG_028126.1:g.5048G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.404G=
ENST00000679326.1:c.-236G= ENSP00000504262.1:n.-236G=
ENST00000260118.6:c.-236G= ENSP00000260118.6:n.-236G=
NM_003878.2:c.-236G= NP_003869.1:n.-236G=
XM_011517623.1:c.-236G= XP_011515925.1:n.-236G=