Canonical Allele Identifier: CA13394433
Gene: PGR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs572483

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101096841T>C , CM000673.2:g.101096841T>C GRCh38
NC_000011.8:g.100472782T>C NCBI36
NC_000011.9:g.100967572T>C , CM000673.1:g.100967572T>C GRCh37
NG_016475.1:g.37973A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263463.9:n.1790-4965A>G ENSP00000263463.5:p.=
ENST00000325455.9:c.1790-4965A>G ENSP00000325120.5:p.=
ENST00000526300.5:n.1790-4965A>G ENSP00000436803.1:p.=
ENST00000528960.5:n.1789+29166A>G ENSP00000432914.1:p.=
ENST00000534013.5:c.8-4965A>G ENSP00000436561.1:p.=
ENST00000534780.5:n.1790-4965A>G ENSP00000432352.1:p.=
ENST00000617858.4:c.1790-4965A>G ENSP00000481227.1:p.=
ENST00000619228.2:c.1789+29166A>G ENSP00000482698.1:p.=
ENST00000632634.1:c.212-4965A>G ENSP00000487607.1:p.=
NM_000926.4:c.1790-4965A>G VV NP_000917.3:p.=
NM_001202474.3:c.1298-4965A>G VV NP_001189403.1:p.=
NM_001271161.2:c.1298-4965A>G VV NP_001258090.1:p.=
NM_001271162.1:c.8-4965A>G VV NP_001258091.1:p.=
NR_073141.2:n.1783-4965A>G
NR_073142.2:n.1782+29166A>G
NR_073143.2:n.1783-4965A>G
XM_006718858.2:c.1790-4965A>G XP_006718921.1:p.=
XR_947831.1:n.3362-4965A>G
XM_006718858.3:c.1790-4965A>G