Canonical Allele Identifier: CA371331273

Gene: GGH

Linked Data

• MyVariant Identifiers: chr8:g.63951237C>G (hg19) ; chr8:g.63038678C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038678C>G , CM000670.2:g.63038678C>G	GRCh38
NC_000008.10:g.63951237C>G , CM000670.1:g.63951237C>G	GRCh37
NC_000008.9:g.64113791C>G	NCBI36
NG_028126.1:g.5374G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260118.7:c.91G>C MANE Select	ENSP00000260118.6:p.Ala31Pro
ENST00000518113.2:c.91G>C	ENSP00000504520.1:p.Ala31Pro
ENST00000523788.2:n.118G>C
ENST00000677327.1:n.730G>C
ENST00000677459.1:c.91G>C	ENSP00000503731.1:p.Ala31Pro
ENST00000677482.1:c.91G>C	ENSP00000504590.1:p.Ala31Pro
ENST00000678069.1:n.125G>C
ENST00000679326.1:c.91G>C	ENSP00000504262.1:p.Ala31Pro
ENST00000260118.6:c.91G>C	ENSP00000260118.6:p.Ala31Pro
ENST00000518966.5:n.124G>C
ENST00000520609.5:n.124G>C
ENST00000523788.1:n.125G>C
NM_003878.2:c.91G>C	NP_003869.1:p.Ala31Pro
XM_011517623.1:c.91G>C	XP_011515925.1:p.Ala31Pro
XM_011517623.3:c.91G>C	XP_011515925.1:p.Ala31Pro
NM_003878.3:c.91G>C MANE Select	NP_003869.1:p.Ala31Pro