Canonical Allele Identifier: CA1995637128
Gene: PGR HGNC NCBI

Linked Data

dbSNP Id: rs1859446447

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101034492T>C , CM000673.2:g.101034492T>C GRCh38
NC_000011.9:g.100905223T>C , CM000673.1:g.100905223T>C GRCh37
NC_000011.8:g.100410433T>C NCBI36
NG_016475.1:g.100322A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000325455.10:c.*4624A>G MANE Select ENSP00000325120.5:n.*4624A>G
ENST00000325455.9:c.*4624A>G ENSP00000325120.5:n.*4624A>G
NM_000926.4:c.*4624A>G MANE Select NP_000917.3:n.*4624A>G
NM_001202474.3:c.*4624A>G NP_001189403.1:n.*4624A>G
NM_001271161.2:c.*4624A>G NP_001258090.1:n.*4624A>G
NM_001271162.1:c.*4624A>G NP_001258091.1:n.*4624A>G
NR_073141.2:n.7367A>G
NR_073142.2:n.7250A>G
NR_073143.2:n.6982A>G
NM_001271162.2:c.*4624A>G NP_001258091.1:n.*4624A>G
NR_073141.3:n.7381A>G
NR_073142.3:n.7264A>G
NR_073143.3:n.6996A>G