Canonical Allele Identifier: CA1788923406

Gene: GGH

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038826C= , CM000670.2:g.63038826C=	GRCh38
NC_000008.10:g.63951385C= , CM000670.1:g.63951385C=	GRCh37
NC_000008.9:g.64113939C=	NCBI36
NG_028126.1:g.5226G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000677327.1:n.582G=
ENST00000677482.1:c.-58G=	ENSP00000504590.1:n.-58G=
ENST00000679326.1:c.-58G=	ENSP00000504262.1:n.-58G=
ENST00000260118.6:c.-58G=	ENSP00000260118.6:n.-58G=
NM_003878.2:c.-58G=	NP_003869.1:n.-58G=
XM_011517623.1:c.-58G=	XP_011515925.1:n.-58G=