Canonical Allele Identifier: CA461138252

Gene: GGH

Linked Data

• gnomAD v4: 8-63038682-G-A
• MyVariant Identifiers: chr8:g.63951241G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038682G>A , CM000670.2:g.63038682G>A	GRCh38
NC_000008.10:g.63951241G>A , CM000670.1:g.63951241G>A	GRCh37
NC_000008.9:g.64113795G>A	NCBI36
NG_028126.1:g.5370C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260118.7:c.87C>T MANE Select	ENSP00000260118.6:p.Asp29=
ENST00000518113.2:c.87C>T	ENSP00000504520.1:p.Asp29=
ENST00000523788.2:n.114C>T
ENST00000677327.1:n.726C>T
ENST00000677459.1:c.87C>T	ENSP00000503731.1:p.Asp29=
ENST00000677482.1:c.87C>T	ENSP00000504590.1:p.Asp29=
ENST00000678069.1:n.121C>T
ENST00000679326.1:c.87C>T	ENSP00000504262.1:p.Asp29=
ENST00000260118.6:c.87C>T	ENSP00000260118.6:p.Asp29=
ENST00000518966.5:n.120C>T
ENST00000520609.5:n.120C>T
ENST00000523788.1:n.121C>T
NM_003878.2:c.87C>T	NP_003869.1:p.Asp29=
XM_011517623.1:c.87C>T	XP_011515925.1:p.Asp29=
XM_011517623.3:c.87C>T	XP_011515925.1:p.Asp29=
NM_003878.3:c.87C>T MANE Select	NP_003869.1:p.Asp29=