Canonical Allele Identifier: CA123481
Gene: PAX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13805
ClinVar RCV Id: RCV000014816
dbSNP Id: rs104894170

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100749914G>C , CM000672.2:g.100749914G>C GRCh38
NC_000010.10:g.102509671G>C , CM000672.1:g.102509671G>C GRCh37
NC_000010.9:g.102499661G>C NCBI36
NG_008680.1:g.9204G>C
NG_008680.2:g.19206G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000707078.1:c.305G>C ENSP00000516729.1:p.Arg102Thr
ENST00000707079.1:c.212G>C ENSP00000516730.1:p.Arg71Thr
ENST00000355243.8:c.212G>C MANE Select ENSP00000347385.3:p.Arg71Thr
ENST00000427256.6:c.212G>C ENSP00000398652.2:p.Arg71Thr
ENST00000679374.1:c.194G>C ENSP00000506041.1:p.Arg65Thr
ENST00000355243.7:c.212G>C ENSP00000347385.2:p.Arg71Thr
ENST00000361791.7:c.209G>C ENSP00000355069.4:p.Arg70Thr
ENST00000370296.6:c.212G>C ENSP00000359319.3:p.Arg71Thr
ENST00000427256.5:c.212G>C ENSP00000398652.1:p.Arg71Thr
ENST00000428433.5:c.212G>C ENSP00000396259.1:p.Arg71Thr
ENST00000483202.2:n.1214G>C
ENST00000553492.5:n.131+14181G>C
ENST00000554172.2:c.224G>C ENSP00000452489.2:p.Arg75Thr
ENST00000554363.2:n.125+3611G>C
NM_000278.3:c.212G>C NP_000269.2:p.Arg71Thr
NM_001304569.1:c.305G>C NP_001291498.1:p.Arg102Thr
NM_003987.3:c.212G>C NP_003978.2:p.Arg71Thr
NM_003988.3:c.212G>C NP_003979.2:p.Arg71Thr
NM_003989.3:c.212G>C NP_003980.2:p.Arg71Thr
NM_003990.3:c.212G>C NP_003981.2:p.Arg71Thr
NM_000278.4:c.212G>C NP_000269.3:p.Arg71Thr
NM_003987.4:c.212G>C NP_003978.3:p.Arg71Thr
NM_003988.4:c.212G>C NP_003979.2:p.Arg71Thr
NM_003989.4:c.212G>C NP_003980.3:p.Arg71Thr
NM_003990.4:c.212G>C NP_003981.3:p.Arg71Thr
NM_000278.5:c.212G>C MANE Select NP_000269.3:p.Arg71Thr
NM_001304569.2:c.305G>C NP_001291498.1:p.Arg102Thr
NM_003987.5:c.212G>C NP_003978.3:p.Arg71Thr
NM_003988.5:c.212G>C NP_003979.2:p.Arg71Thr
NM_003989.5:c.212G>C NP_003980.3:p.Arg71Thr
NM_003990.5:c.212G>C NP_003981.3:p.Arg71Thr