Canonical Allele Identifier: CA6243389
Gene: PGR HGNC NCBI
gnomAD v2:
11:100909809 A / G
gnomAD v3:
11:101039078 A / G
gnomAD v4:
chr11-101039078-A-G
Joint Max Group AF 0.38691188 (AFR)
Genomes Max Group AF 0.38893656 (AFR)
Exomes Max Group AF 0.38076018 (AFR)
dbSNP:
484389
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101039078A>G , CM000673.2:g.101039078A>G GRCh38
NC_000011.9:g.100909809A>G , CM000673.1:g.100909809A>G GRCh37
NC_000011.8:g.100415019A>G NCBI36
NG_016475.1:g.95736T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.*38T>C MANE Select ENSP00000325120.5:n.*38T>C
ENST00000325455.9:c.*38T>C ENSP00000325120.5:n.*38T>C
ENST00000533207.5:n.2207T>C
ENST00000534013.5:c.*38T>C ENSP00000436561.1:n.*38T>C
NM_000926.4:c.*38T>C MANE Select NP_000917.3:n.*38T>C
NM_001202474.3:c.*38T>C NP_001189403.1:n.*38T>C
NM_001271161.2:c.*38T>C NP_001258090.1:n.*38T>C
NM_001271162.1:c.*38T>C NP_001258091.1:n.*38T>C
NR_073141.2:n.2781T>C
NR_073142.2:n.2664T>C
NR_073143.2:n.2396T>C
NM_001271162.2:c.*38T>C NP_001258091.1:n.*38T>C
NR_073141.3:n.2795T>C
NR_073142.3:n.2678T>C
NR_073143.3:n.2410T>C
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