Canonical Allele Identifier: CA1788923594
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039076T= , CM000670.2:g.63039076T= GRCh38
NC_000008.10:g.63951635T= , CM000670.1:g.63951635T= GRCh37
NC_000008.9:g.64114189T= NCBI36
NG_028126.1:g.4976A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.332A=
ENST00000679326.1:c.-308A= ENSP00000504262.1:n.-308A=
ENST00000260118.6:c.-308A= ENSP00000260118.6:n.-308A=
XM_011517623.1:c.-308A= XP_011515925.1:n.-308A=