Canonical Allele Identifier: CA362707920

Gene: GCNT2

Linked Data

• dbSNP Id: rs1761362389
• gnomAD v3: 6-10529377-A-G
• gnomAD v4: 6-10529377-A-G
• MyVariant Identifiers: chr6:g.10529610A>G (hg19) ; chr6:g.10529377A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529377A>G , CM000668.2:g.10529377A>G	GRCh38
NC_000006.11:g.10529610A>G , CM000668.1:g.10529610A>G	GRCh37
NC_000006.10:g.10637596A>G	NCBI36
NG_007469.3:g.42155A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+536A>G
ENST00000495262.7:c.466A>G MANE Select	ENSP00000419411.2:p.Lys156Glu
ENST00000379597.7:c.466A>G	ENSP00000368917.3:p.Lys156Glu
ENST00000397423.6:n.484+536A>G
ENST00000410107.5:c.67+20219A>G	ENSP00000386321.1:n.67+20219A>G
ENST00000474518.1:n.508+536A>G
ENST00000474983.5:n.1043A>G
ENST00000475577.5:n.254+1717A>G
ENST00000483204.1:n.1042A>G
ENST00000489225.5:n.283+36446A>G
ENST00000489819.5:n.175+7783A>G
ENST00000495262.5:c.466A>G	ENSP00000419411.1:p.Lys156Glu
NM_145649.4:c.466A>G	NP_663624.1:p.Lys156Glu
XM_005248999.2:c.235A>G	XP_005249056.1:p.Lys79Glu
XM_006715052.2:c.466A>G	XP_006715115.1:p.Lys156Glu
XM_006715053.2:c.466A>G	XP_006715116.1:p.Lys156Glu
XM_011514465.1:c.466A>G	XP_011512767.1:p.Lys156Glu
XM_011514467.1:c.235A>G	XP_011512769.1:p.Lys79Glu
XM_011514468.1:c.466A>G	XP_011512770.1:p.Lys156Glu
XR_926136.1:n.1017A>G
XM_006715052.3:c.466A>G	XP_006715115.1:p.Lys156Glu
XM_011514468.3:c.466A>G	XP_011512770.1:p.Lys156Glu
XM_017010732.2:c.466A>G	XP_016866221.1:p.Lys156Glu
XR_002956275.1:n.1017A>G
XR_926136.2:n.1015A>G
NM_001374747.1:c.466A>G	NP_001361676.1:p.Lys156Glu
NM_145649.5:c.466A>G MANE Select	NP_663624.1:p.Lys156Glu