Canonical Allele Identifier: CA1114587600

Gene: GGH

Linked Data

• dbSNP Id: rs1804970500
• gnomAD v3: 8-63038967-TGC-T
• gnomAD v4: 8-63038967-TGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038972_63038973del , CM000670.2:g.63038972_63038973del	GRCh38
NC_000008.10:g.63951531_63951532del , CM000670.1:g.63951531_63951532del	GRCh37
NC_000008.9:g.64114085_64114086del	NCBI36
NG_028126.1:g.5083_5084del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000677327.1:n.439_440del
ENST00000679326.1:c.-201_-200del	ENSP00000504262.1:n.-201_-200del
ENST00000260118.6:c.-201_-200del	ENSP00000260118.6:n.-201_-200del
NM_003878.2:c.-201_-200del	NP_003869.1:n.-201_-200del
XM_011517623.1:c.-201_-200del	XP_011515925.1:n.-201_-200del