Canonical Allele Identifier: CA227513667
Gene: PGR HGNC NCBI

Linked Data

dbSNP Id: rs554815610

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101034501T>C , CM000673.2:g.101034501T>C GRCh38
NC_000011.9:g.100905232T>C , CM000673.1:g.100905232T>C GRCh37
NC_000011.8:g.100410442T>C NCBI36
NG_016475.1:g.100313A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000325455.10:c.*4615A>G MANE Select ENSP00000325120.5:n.*4615A>G
ENST00000325455.9:c.*4615A>G ENSP00000325120.5:n.*4615A>G
NM_000926.4:c.*4615A>G MANE Select NP_000917.3:n.*4615A>G
NM_001202474.3:c.*4615A>G NP_001189403.1:n.*4615A>G
NM_001271161.2:c.*4615A>G NP_001258090.1:n.*4615A>G
NM_001271162.1:c.*4615A>G NP_001258091.1:n.*4615A>G
NR_073141.2:n.7358A>G
NR_073142.2:n.7241A>G
NR_073143.2:n.6973A>G
NM_001271162.2:c.*4615A>G NP_001258091.1:n.*4615A>G
NR_073141.3:n.7372A>G
NR_073142.3:n.7255A>G
NR_073143.3:n.6987A>G