Canonical Allele Identifier: CA670697055

Gene: PGR

Linked Data

• dbSNP Id: rs1453907524
• gnomAD v3: 11-101034545-G-C
• gnomAD v4: 11-101034545-G-C
• MyVariant Identifiers: chr11:g.100905276G>C (hg19) ; chr11:g.101034545G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034545G>C , CM000673.2:g.101034545G>C	GRCh38
NC_000011.9:g.100905276G>C , CM000673.1:g.100905276G>C	GRCh37
NC_000011.8:g.100410486G>C	NCBI36
NG_016475.1:g.100269C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4571C>G MANE Select	ENSP00000325120.5:n.*4571C>G
ENST00000325455.9:c.*4571C>G	ENSP00000325120.5:n.*4571C>G
NM_000926.4:c.*4571C>G MANE Select	NP_000917.3:n.*4571C>G
NM_001202474.3:c.*4571C>G	NP_001189403.1:n.*4571C>G
NM_001271161.2:c.*4571C>G	NP_001258090.1:n.*4571C>G
NM_001271162.1:c.*4571C>G	NP_001258091.1:n.*4571C>G
NR_073141.2:n.7314C>G
NR_073142.2:n.7197C>G
NR_073143.2:n.6929C>G
NM_001271162.2:c.*4571C>G	NP_001258091.1:n.*4571C>G
NR_073141.3:n.7328C>G
NR_073142.3:n.7211C>G
NR_073143.3:n.6943C>G