Canonical Allele Identifier: CA1788923521

Gene: GGH

Linked Data

• dbSNP Id: rs1804970500

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038970_63038973dup , CM000670.2:g.63038970_63038973dup	GRCh38
NC_000008.10:g.63951529_63951532dup , CM000670.1:g.63951529_63951532dup	GRCh37
NC_000008.9:g.64114083_64114086dup	NCBI36
NG_028126.1:g.5081_5084dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000677327.1:n.437_440dup
ENST00000679326.1:c.-203_-200dup	ENSP00000504262.1:n.-203_-200dup
ENST00000260118.6:c.-203_-200dup	ENSP00000260118.6:n.-203_-200dup
NM_003878.2:c.-203_-200dup	NP_003869.1:n.-203_-200dup
XM_011517623.1:c.-203_-200dup	XP_011515925.1:n.-203_-200dup