Canonical Allele Identifier: CA1788923559
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039017C= , CM000670.2:g.63039017C= GRCh38
NC_000008.10:g.63951576C= , CM000670.1:g.63951576C= GRCh37
NC_000008.9:g.64114130C= NCBI36
NG_028126.1:g.5035G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.391G=
ENST00000679326.1:c.-249G= ENSP00000504262.1:n.-249G=
ENST00000260118.6:c.-249G= ENSP00000260118.6:n.-249G=
NM_003878.2:c.-249G= NP_003869.1:n.-249G=
XM_011517623.1:c.-249G= XP_011515925.1:n.-249G=