Canonical Allele Identifier: CA2687440026

Gene: GGH

Linked Data

• gnomAD v4: 8-63038836-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038837del , CM000670.2:g.63038837del	GRCh38
NC_000008.10:g.63951396del , CM000670.1:g.63951396del	GRCh37
NC_000008.9:g.64113950del	NCBI36
NG_028126.1:g.5215del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000677327.1:n.571del
ENST00000677482.1:c.-69del	ENSP00000504590.1:n.-69del
ENST00000679326.1:c.-69del	ENSP00000504262.1:n.-69del
ENST00000260118.6:c.-69del	ENSP00000260118.6:n.-69del
NM_003878.2:c.-69del	NP_003869.1:n.-69del
XM_011517623.1:c.-69del	XP_011515925.1:n.-69del