Canonical Allele Identifier: CA1788923513
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038960C= , CM000670.2:g.63038960C= GRCh38
NC_000008.10:g.63951519C= , CM000670.1:g.63951519C= GRCh37
NC_000008.9:g.64114073C= NCBI36
NG_028126.1:g.5092G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.448G=
ENST00000679326.1:c.-192G= ENSP00000504262.1:n.-192G=
ENST00000260118.6:c.-192G= ENSP00000260118.6:n.-192G=
NM_003878.2:c.-192G= NP_003869.1:n.-192G=
XM_011517623.1:c.-192G= XP_011515925.1:n.-192G=