Canonical Allele Identifier: CA1788923586
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039069T= , CM000670.2:g.63039069T= GRCh38
NC_000008.10:g.63951628T= , CM000670.1:g.63951628T= GRCh37
NC_000008.9:g.64114182T= NCBI36
NG_028126.1:g.4983A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.339A=
ENST00000679326.1:c.-301A= ENSP00000504262.1:n.-301A=
ENST00000260118.6:c.-301A= ENSP00000260118.6:n.-301A=
XM_011517623.1:c.-301A= XP_011515925.1:n.-301A=