Canonical Allele Identifier: CA1788923619
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039120T= , CM000670.2:g.63039120T= GRCh38
NC_000008.10:g.63951679T= , CM000670.1:g.63951679T= GRCh37
NC_000008.9:g.64114233T= NCBI36
NG_028126.1:g.4932A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.288A=
ENST00000679326.1:c.-352A= ENSP00000504262.1:n.-352A=
ENST00000260118.6:c.-352A= ENSP00000260118.6:n.-352A=
XM_011517623.1:c.-352A= XP_011515925.1:n.-352A=