Canonical Allele Identifier: CA13427091

Gene: PGR

Linked Data

• dbSNP Id: rs11224561
• gnomAD v2: 11-100905056-C-T
• gnomAD v3: 11-101034325-C-T
• gnomAD v4: 11-101034325-C-T
• MyVariant Identifiers: chr11:g.100905056C>T (hg19) ; chr11:g.101034325C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034325C>T , CM000673.2:g.101034325C>T	GRCh38
NC_000011.9:g.100905056C>T , CM000673.1:g.100905056C>T	GRCh37
NC_000011.8:g.100410266C>T	NCBI36
NG_016475.1:g.100489G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.*4791G>A MANE Select	ENSP00000325120.5:n.*4791G>A
ENST00000325455.9:c.*4791G>A	ENSP00000325120.5:n.*4791G>A
NM_000926.4:c.*4791G>A MANE Select	NP_000917.3:n.*4791G>A
NM_001202474.3:c.*4791G>A	NP_001189403.1:n.*4791G>A
NM_001271161.2:c.*4791G>A	NP_001258090.1:n.*4791G>A
NM_001271162.1:c.*4791G>A	NP_001258091.1:n.*4791G>A
NR_073141.2:n.7534G>A
NR_073142.2:n.7417G>A
NR_073143.2:n.7149G>A
NM_001271162.2:c.*4791G>A	NP_001258091.1:n.*4791G>A
NR_073141.3:n.7548G>A
NR_073142.3:n.7431G>A
NR_073143.3:n.7163G>A