Canonical Allele Identifier: CA2687440122

Gene: GGH

Linked Data

• gnomAD v4: 8-63038905-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038908del , CM000670.2:g.63038908del	GRCh38
NC_000008.10:g.63951467del , CM000670.1:g.63951467del	GRCh37
NC_000008.9:g.64114021del	NCBI36
NG_028126.1:g.5146del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000677327.1:n.502del
ENST00000679326.1:c.-138del	ENSP00000504262.1:n.-138del
ENST00000260118.6:c.-138del	ENSP00000260118.6:n.-138del
NM_003878.2:c.-138del	NP_003869.1:n.-138del
XM_011517623.1:c.-138del	XP_011515925.1:n.-138del