Canonical Allele Identifier: CA1788923533
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038989G= , CM000670.2:g.63038989G= GRCh38
NC_000008.10:g.63951548G= , CM000670.1:g.63951548G= GRCh37
NC_000008.9:g.64114102G= NCBI36
NG_028126.1:g.5063C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.419C=
ENST00000679326.1:c.-221C= ENSP00000504262.1:n.-221C=
ENST00000260118.6:c.-221C= ENSP00000260118.6:n.-221C=
NM_003878.2:c.-221C= NP_003869.1:n.-221C=
XM_011517623.1:c.-221C= XP_011515925.1:n.-221C=