Canonical Allele Identifier: CA2687440161

Gene: GGH

Linked Data

• gnomAD v4: 8-63038928-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038932del , CM000670.2:g.63038932del	GRCh38
NC_000008.10:g.63951491del , CM000670.1:g.63951491del	GRCh37
NC_000008.9:g.64114045del	NCBI36
NG_028126.1:g.5123del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000677327.1:n.479del
ENST00000679326.1:c.-161del	ENSP00000504262.1:n.-161del
ENST00000260118.6:c.-161del	ENSP00000260118.6:n.-161del
NM_003878.2:c.-161del	NP_003869.1:n.-161del
XM_011517623.1:c.-161del	XP_011515925.1:n.-161del