Canonical Allele Identifier: CA178366988

Gene: GGH

Linked Data

• dbSNP Id: rs889812120
• gnomAD v2: 8-63951512-A-T
• gnomAD v3: 8-63038953-A-T
• gnomAD v4: 8-63038953-A-T
• MyVariant Identifiers: chr8:g.63951512A>T (hg19) ; chr8:g.63038953A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038953A>T , CM000670.2:g.63038953A>T	GRCh38
NC_000008.10:g.63951512A>T , CM000670.1:g.63951512A>T	GRCh37
NC_000008.9:g.64114066A>T	NCBI36
NG_028126.1:g.5099T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000677327.1:n.455T>A
ENST00000679326.1:c.-185T>A	ENSP00000504262.1:n.-185T>A
ENST00000260118.6:c.-185T>A	ENSP00000260118.6:n.-185T>A
NM_003878.2:c.-185T>A	NP_003869.1:n.-185T>A
XM_011517623.1:c.-185T>A	XP_011515925.1:n.-185T>A