Canonical Allele Identifier: CA448718270

Gene: GCNT2

Linked Data

• MyVariant Identifiers: chr6:g.10529831T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529598T>G , CM000668.2:g.10529598T>G	GRCh38
NC_000006.11:g.10529831T>G , CM000668.1:g.10529831T>G	GRCh37
NC_000006.10:g.10637817T>G	NCBI36
NG_007469.3:g.42376T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000397423.7:n.484+757T>G
ENST00000495262.7:c.687T>G MANE Select	ENSP00000419411.2:p.Thr229=
ENST00000379597.7:c.687T>G	ENSP00000368917.3:p.Thr229=
ENST00000397423.6:n.484+757T>G
ENST00000410107.5:c.67+20440T>G	ENSP00000386321.1:n.67+20440T>G
ENST00000474518.1:n.508+757T>G
ENST00000474983.5:n.1264T>G
ENST00000475577.5:n.254+1938T>G
ENST00000483204.1:n.1263T>G
ENST00000489225.5:n.283+36667T>G
ENST00000489819.5:n.175+8004T>G
ENST00000495262.5:c.687T>G	ENSP00000419411.1:p.Thr229=
NM_145649.4:c.687T>G	NP_663624.1:p.Thr229=
XM_005248999.2:c.456T>G	XP_005249056.1:p.Thr152=
XM_006715052.2:c.687T>G	XP_006715115.1:p.Thr229=
XM_006715053.2:c.687T>G	XP_006715116.1:p.Thr229=
XM_011514465.1:c.687T>G	XP_011512767.1:p.Thr229=
XM_011514467.1:c.456T>G	XP_011512769.1:p.Thr152=
XM_011514468.1:c.687T>G	XP_011512770.1:p.Thr229=
XR_926136.1:n.1238T>G
XM_006715052.3:c.687T>G	XP_006715115.1:p.Thr229=
XM_011514468.3:c.687T>G	XP_011512770.1:p.Thr229=
XM_017010732.2:c.687T>G	XP_016866221.1:p.Thr229=
XR_002956275.1:n.1238T>G
XR_926136.2:n.1236T>G
NM_001374747.1:c.687T>G	NP_001361676.1:p.Thr229=
NM_145649.5:c.687T>G MANE Select	NP_663624.1:p.Thr229=