Canonical Allele Identifier: CA227513630

Gene: PGR

Linked Data

• dbSNP Id: rs940784905
• gnomAD v2: 11-100905125-G-A
• gnomAD v3: 11-101034394-G-A
• gnomAD v4: 11-101034394-G-A
• MyVariant Identifiers: chr11:g.100905125G>A (hg19) ; chr11:g.101034394G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034394G>A , CM000673.2:g.101034394G>A	GRCh38
NC_000011.9:g.100905125G>A , CM000673.1:g.100905125G>A	GRCh37
NC_000011.8:g.100410335G>A	NCBI36
NG_016475.1:g.100420C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.*4722C>T MANE Select	ENSP00000325120.5:n.*4722C>T
ENST00000325455.9:c.*4722C>T	ENSP00000325120.5:n.*4722C>T
NM_000926.4:c.*4722C>T MANE Select	NP_000917.3:n.*4722C>T
NM_001202474.3:c.*4722C>T	NP_001189403.1:n.*4722C>T
NM_001271161.2:c.*4722C>T	NP_001258090.1:n.*4722C>T
NM_001271162.1:c.*4722C>T	NP_001258091.1:n.*4722C>T
NR_073141.2:n.7465C>T
NR_073142.2:n.7348C>T
NR_073143.2:n.7080C>T
NM_001271162.2:c.*4722C>T	NP_001258091.1:n.*4722C>T
NR_073141.3:n.7479C>T
NR_073142.3:n.7362C>T
NR_073143.3:n.7094C>T