Canonical Allele Identifier: CA1788923495
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038941G= , CM000670.2:g.63038941G= GRCh38
NC_000008.10:g.63951500G= , CM000670.1:g.63951500G= GRCh37
NC_000008.9:g.64114054G= NCBI36
NG_028126.1:g.5111C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.467C=
ENST00000679326.1:c.-173C= ENSP00000504262.1:n.-173C=
ENST00000260118.6:c.-173C= ENSP00000260118.6:n.-173C=
NM_003878.2:c.-173C= NP_003869.1:n.-173C=
XM_011517623.1:c.-173C= XP_011515925.1:n.-173C=