Canonical Allele Identifier: CA1788923439

Gene: GGH

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038860C= , CM000670.2:g.63038860C=	GRCh38
NC_000008.10:g.63951419C= , CM000670.1:g.63951419C=	GRCh37
NC_000008.9:g.64113973C=	NCBI36
NG_028126.1:g.5192G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000677327.1:n.548G=
ENST00000677482.1:c.-92G=	ENSP00000504590.1:n.-92G=
ENST00000679326.1:c.-92G=	ENSP00000504262.1:n.-92G=
ENST00000260118.6:c.-92G=	ENSP00000260118.6:n.-92G=
NM_003878.2:c.-92G=	NP_003869.1:n.-92G=
XM_011517623.1:c.-92G=	XP_011515925.1:n.-92G=