Canonical Allele Identifier: CA658858793
Gene: PAX2 HGNC NCBI

Linked Data

dbSNP Id: rs1458822798

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100749678C>T , CM000672.2:g.100749678C>T GRCh38
NC_000010.10:g.102509435C>T , CM000672.1:g.102509435C>T GRCh37
NC_000010.9:g.102499425C>T NCBI36
NG_008680.1:g.8968C>T
NG_008680.2:g.18970C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000707078.1:c.137-68C>T ENSP00000516729.1:n.137-68C>T
ENST00000707079.1:c.44-68C>T ENSP00000516730.1:n.44-68C>T
ENST00000355243.8:c.44-68C>T MANE Select ENSP00000347385.3:n.44-68C>T
ENST00000427256.6:c.44-68C>T ENSP00000398652.2:n.44-68C>T
ENST00000679374.1:c.26-68C>T ENSP00000506041.1:n.26-68C>T
ENST00000355243.7:c.44-68C>T ENSP00000347385.2:n.44-68C>T
ENST00000361791.7:c.44-71C>T ENSP00000355069.4:n.44-71C>T
ENST00000370296.6:c.44-68C>T ENSP00000359319.3:n.44-68C>T
ENST00000427256.5:c.44-68C>T ENSP00000398652.1:n.44-68C>T
ENST00000428433.5:c.44-68C>T ENSP00000396259.1:n.44-68C>T
ENST00000483202.2:n.1046-68C>T
ENST00000553492.5:n.131+13945C>T
ENST00000554172.2:c.-13C>T ENSP00000452489.2:n.-13C>T
ENST00000554363.2:n.125+3375C>T
NM_000278.3:c.44-68C>T NP_000269.2:n.44-68C>T
NM_001304569.1:c.137-68C>T NP_001291498.1:n.137-68C>T
NM_003987.3:c.44-68C>T NP_003978.2:n.44-68C>T
NM_003988.3:c.44-68C>T NP_003979.2:n.44-68C>T
NM_003989.3:c.44-68C>T NP_003980.2:n.44-68C>T
NM_003990.3:c.44-68C>T NP_003981.2:n.44-68C>T
NM_000278.4:c.44-68C>T NP_000269.3:n.44-68C>T
NM_003987.4:c.44-68C>T NP_003978.3:n.44-68C>T
NM_003988.4:c.44-68C>T NP_003979.2:n.44-68C>T
NM_003989.4:c.44-68C>T NP_003980.3:n.44-68C>T
NM_003990.4:c.44-68C>T NP_003981.3:n.44-68C>T
NM_000278.5:c.44-68C>T MANE Select NP_000269.3:n.44-68C>T
NM_001304569.2:c.137-68C>T NP_001291498.1:n.137-68C>T
NM_003987.5:c.44-68C>T NP_003978.3:n.44-68C>T
NM_003988.5:c.44-68C>T NP_003979.2:n.44-68C>T
NM_003989.5:c.44-68C>T NP_003980.3:n.44-68C>T
NM_003990.5:c.44-68C>T NP_003981.3:n.44-68C>T