Canonical Allele Identifier: CA601422367

Gene: PGR

Linked Data

• dbSNP Id: rs368300047
• gnomAD v2: 11-100905300-C-G
• gnomAD v3: 11-101034569-C-G
• gnomAD v4: 11-101034569-C-G
• MyVariant Identifiers: chr11:g.100905300C>G (hg19) ; chr11:g.101034569C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034569C>G , CM000673.2:g.101034569C>G	GRCh38
NC_000011.9:g.100905300C>G , CM000673.1:g.100905300C>G	GRCh37
NC_000011.8:g.100410510C>G	NCBI36
NG_016475.1:g.100245G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4547G>C MANE Select	ENSP00000325120.5:n.*4547G>C
ENST00000325455.9:c.*4547G>C	ENSP00000325120.5:n.*4547G>C
NM_000926.4:c.*4547G>C MANE Select	NP_000917.3:n.*4547G>C
NM_001202474.3:c.*4547G>C	NP_001189403.1:n.*4547G>C
NM_001271161.2:c.*4547G>C	NP_001258090.1:n.*4547G>C
NM_001271162.1:c.*4547G>C	NP_001258091.1:n.*4547G>C
NR_073141.2:n.7290G>C
NR_073142.2:n.7173G>C
NR_073143.2:n.6905G>C
NM_001271162.2:c.*4547G>C	NP_001258091.1:n.*4547G>C
NR_073141.3:n.7304G>C
NR_073142.3:n.7187G>C
NR_073143.3:n.6919G>C