Canonical Allele Identifier: CA1995637167

Gene: PGR

Linked Data

• dbSNP Id: rs1859450379

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034591T>C , CM000673.2:g.101034591T>C	GRCh38
NC_000011.9:g.100905322T>C , CM000673.1:g.100905322T>C	GRCh37
NC_000011.8:g.100410532T>C	NCBI36
NG_016475.1:g.100223A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.*4525A>G MANE Select	ENSP00000325120.5:n.*4525A>G
ENST00000325455.9:c.*4525A>G	ENSP00000325120.5:n.*4525A>G
NM_000926.4:c.*4525A>G MANE Select	NP_000917.3:n.*4525A>G
NM_001202474.3:c.*4525A>G	NP_001189403.1:n.*4525A>G
NM_001271161.2:c.*4525A>G	NP_001258090.1:n.*4525A>G
NM_001271162.1:c.*4525A>G	NP_001258091.1:n.*4525A>G
NR_073141.2:n.7268A>G
NR_073142.2:n.7151A>G
NR_073143.2:n.6883A>G
NM_001271162.2:c.*4525A>G	NP_001258091.1:n.*4525A>G
NR_073141.3:n.7282A>G
NR_073142.3:n.7165A>G
NR_073143.3:n.6897A>G