Canonical Allele Identifier: CA1788923441

Gene: GGH

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038863G= , CM000670.2:g.63038863G=	GRCh38
NC_000008.10:g.63951422G= , CM000670.1:g.63951422G=	GRCh37
NC_000008.9:g.64113976G=	NCBI36
NG_028126.1:g.5189C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000677327.1:n.545C=
ENST00000677482.1:c.-95C=	ENSP00000504590.1:n.-95C=
ENST00000679326.1:c.-95C=	ENSP00000504262.1:n.-95C=
ENST00000260118.6:c.-95C=	ENSP00000260118.6:n.-95C=
NM_003878.2:c.-95C=	NP_003869.1:n.-95C=
XM_011517623.1:c.-95C=	XP_011515925.1:n.-95C=