Canonical Allele Identifier: CA2687440149

Gene: GGH

Linked Data

• gnomAD v4: 8-63038919-AGGCGGCCGTGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038926_63038936del , CM000670.2:g.63038926_63038936del	GRCh38
NC_000008.10:g.63951485_63951495del , CM000670.1:g.63951485_63951495del	GRCh37
NC_000008.9:g.64114039_64114049del	NCBI36
NG_028126.1:g.5122_5132del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000677327.1:n.478_488del
ENST00000679326.1:c.-162_-152del	ENSP00000504262.1:n.-162_-152del
ENST00000260118.6:c.-162_-152del	ENSP00000260118.6:n.-162_-152del
NM_003878.2:c.-162_-152del	NP_003869.1:n.-162_-152del
XM_011517623.1:c.-162_-152del	XP_011515925.1:n.-162_-152del