Canonical Allele Identifier: CA3631799
Gene: GCNT2 HGNC NCBI

Linked Data

dbSNP Id: rs753331219
gnomAD v2: 6-10529808-C-T
gnomAD v3: 6-10529575-C-T
gnomAD v4: 6-10529575-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10529575C>T , CM000668.2:g.10529575C>T GRCh38
NC_000006.11:g.10529808C>T , CM000668.1:g.10529808C>T GRCh37
NC_000006.10:g.10637794C>T NCBI36
NG_007469.3:g.42353C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000397423.7:n.484+734C>T
ENST00000495262.7:c.664C>T MANE Select ENSP00000419411.2:p.Pro222Ser
ENST00000379597.7:c.664C>T ENSP00000368917.3:p.Pro222Ser
ENST00000397423.6:n.484+734C>T
ENST00000410107.5:c.67+20417C>T ENSP00000386321.1:n.67+20417C>T
ENST00000474518.1:n.508+734C>T
ENST00000474983.5:n.1241C>T
ENST00000475577.5:n.254+1915C>T
ENST00000483204.1:n.1240C>T
ENST00000489225.5:n.283+36644C>T
ENST00000489819.5:n.175+7981C>T
ENST00000495262.5:c.664C>T ENSP00000419411.1:p.Pro222Ser
NM_145649.4:c.664C>T NP_663624.1:p.Pro222Ser
XM_005248999.2:c.433C>T XP_005249056.1:p.Pro145Ser
XM_006715052.2:c.664C>T XP_006715115.1:p.Pro222Ser
XM_006715053.2:c.664C>T XP_006715116.1:p.Pro222Ser
XM_011514465.1:c.664C>T XP_011512767.1:p.Pro222Ser
XM_011514467.1:c.433C>T XP_011512769.1:p.Pro145Ser
XM_011514468.1:c.664C>T XP_011512770.1:p.Pro222Ser
XR_926136.1:n.1215C>T
XM_006715052.3:c.664C>T XP_006715115.1:p.Pro222Ser
XM_011514468.3:c.664C>T XP_011512770.1:p.Pro222Ser
XM_017010732.2:c.664C>T XP_016866221.1:p.Pro222Ser
XR_002956275.1:n.1215C>T
XR_926136.2:n.1213C>T
NM_001374747.1:c.664C>T NP_001361676.1:p.Pro222Ser
NM_145649.5:c.664C>T MANE Select NP_663624.1:p.Pro222Ser