Canonical Allele Identifier: CA4763115

Gene: GGH

Linked Data

• dbSNP Id: rs766118226
• ExAC: 8:63951318 G / A
• gnomAD v2: 8-63951318-G-A
• gnomAD v3: 8-63038759-G-A
• gnomAD v4: 8-63038759-G-A
• MyVariant Identifiers: chr8:g.63951318G>A (hg19) ; chr8:g.63038759G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038759G>A , CM000670.2:g.63038759G>A	GRCh38
NC_000008.10:g.63951318G>A , CM000670.1:g.63951318G>A	GRCh37
NC_000008.9:g.64113872G>A	NCBI36
NG_028126.1:g.5293C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260118.7:c.10C>T MANE Select	ENSP00000260118.6:p.Pro4Ser
ENST00000518113.2:c.10C>T	ENSP00000504520.1:p.Pro4Ser
ENST00000523788.2:n.37C>T
ENST00000677327.1:n.649C>T
ENST00000677459.1:c.10C>T	ENSP00000503731.1:p.Pro4Ser
ENST00000677482.1:c.10C>T	ENSP00000504590.1:p.Pro4Ser
ENST00000678069.1:n.44C>T
ENST00000679326.1:c.10C>T	ENSP00000504262.1:p.Pro4Ser
ENST00000260118.6:c.10C>T	ENSP00000260118.6:p.Pro4Ser
ENST00000518966.5:n.43C>T
ENST00000520609.5:n.43C>T
ENST00000523788.1:n.44C>T
NM_003878.2:c.10C>T	NP_003869.1:p.Pro4Ser
XM_011517623.1:c.10C>T	XP_011515925.1:p.Pro4Ser
XM_011517623.3:c.10C>T	XP_011515925.1:p.Pro4Ser
NM_003878.3:c.10C>T MANE Select	NP_003869.1:p.Pro4Ser