Canonical Allele Identifier: CA1788923375

Gene: GGH

Linked Data

• dbSNP Id: rs1804964823

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038795C>T , CM000670.2:g.63038795C>T	GRCh38
NC_000008.10:g.63951354C>T , CM000670.1:g.63951354C>T	GRCh37
NC_000008.9:g.64113908C>T	NCBI36
NG_028126.1:g.5257G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260118.7:c.-27G>A MANE Select	ENSP00000260118.6:n.-27G>A
ENST00000518113.2:c.-27G>A	ENSP00000504520.1:n.-27G>A
ENST00000523788.2:n.1G>A
ENST00000677327.1:n.613G>A
ENST00000677459.1:c.-27G>A	ENSP00000503731.1:n.-27G>A
ENST00000677482.1:c.-27G>A	ENSP00000504590.1:n.-27G>A
ENST00000678069.1:n.8G>A
ENST00000679326.1:c.-27G>A	ENSP00000504262.1:n.-27G>A
ENST00000260118.6:c.-27G>A	ENSP00000260118.6:n.-27G>A
ENST00000518966.5:n.7G>A
ENST00000520609.5:n.7G>A
ENST00000523788.1:n.8G>A
NM_003878.2:c.-27G>A	NP_003869.1:n.-27G>A
XM_011517623.1:c.-27G>A	XP_011515925.1:n.-27G>A
XM_011517623.3:c.-27G>A	XP_011515925.1:n.-27G>A
NM_003878.3:c.-27G>A MANE Select	NP_003869.1:n.-27G>A