Canonical Allele Identifier: CA1788923598
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039078G= , CM000670.2:g.63039078G= GRCh38
NC_000008.10:g.63951637G= , CM000670.1:g.63951637G= GRCh37
NC_000008.9:g.64114191G= NCBI36
NG_028126.1:g.4974C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.330C=
ENST00000679326.1:c.-310C= ENSP00000504262.1:n.-310C=
ENST00000260118.6:c.-310C= ENSP00000260118.6:n.-310C=
XM_011517623.1:c.-310C= XP_011515925.1:n.-310C=