Canonical Allele Identifier: CA941512627

Gene: PGR

Linked Data

• dbSNP Id: rs1859455681
• gnomAD v3: 11-101034750-T-C
• gnomAD v4: 11-101034750-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034750T>C , CM000673.2:g.101034750T>C	GRCh38
NC_000011.9:g.100905481T>C , CM000673.1:g.100905481T>C	GRCh37
NC_000011.8:g.100410691T>C	NCBI36
NG_016475.1:g.100064A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4366A>G MANE Select	ENSP00000325120.5:n.*4366A>G
ENST00000325455.9:c.*4366A>G	ENSP00000325120.5:n.*4366A>G
NM_000926.4:c.*4366A>G MANE Select	NP_000917.3:n.*4366A>G
NM_001202474.3:c.*4366A>G	NP_001189403.1:n.*4366A>G
NM_001271161.2:c.*4366A>G	NP_001258090.1:n.*4366A>G
NM_001271162.1:c.*4366A>G	NP_001258091.1:n.*4366A>G
NR_073141.2:n.7109A>G
NR_073142.2:n.6992A>G
NR_073143.2:n.6724A>G
NM_001271162.2:c.*4366A>G	NP_001258091.1:n.*4366A>G
NR_073141.3:n.7123A>G
NR_073142.3:n.7006A>G
NR_073143.3:n.6738A>G