Canonical Allele Identifier: CA1788923442

Gene: GGH

Linked Data

• dbSNP Id: rs949744003
• gnomAD v4: 8-63038863-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038863G>A , CM000670.2:g.63038863G>A	GRCh38
NC_000008.10:g.63951422G>A , CM000670.1:g.63951422G>A	GRCh37
NC_000008.9:g.64113976G>A	NCBI36
NG_028126.1:g.5189C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000677327.1:n.545C>T
ENST00000677482.1:c.-95C>T	ENSP00000504590.1:n.-95C>T
ENST00000679326.1:c.-95C>T	ENSP00000504262.1:n.-95C>T
ENST00000260118.6:c.-95C>T	ENSP00000260118.6:n.-95C>T
NM_003878.2:c.-95C>T	NP_003869.1:n.-95C>T
XM_011517623.1:c.-95C>T	XP_011515925.1:n.-95C>T