Canonical Allele Identifier: CA601422349

Gene: PGR

Linked Data

• dbSNP Id: rs1225884294
• gnomAD v2: 11-100905218-T-C
• MyVariant Identifiers: chr11:g.100905218T>C (hg19) ; chr11:g.101034487T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034487T>C , CM000673.2:g.101034487T>C	GRCh38
NC_000011.9:g.100905218T>C , CM000673.1:g.100905218T>C	GRCh37
NC_000011.8:g.100410428T>C	NCBI36
NG_016475.1:g.100327A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.*4629A>G MANE Select	ENSP00000325120.5:n.*4629A>G
ENST00000325455.9:c.*4629A>G	ENSP00000325120.5:n.*4629A>G
NM_000926.4:c.*4629A>G MANE Select	NP_000917.3:n.*4629A>G
NM_001202474.3:c.*4629A>G	NP_001189403.1:n.*4629A>G
NM_001271161.2:c.*4629A>G	NP_001258090.1:n.*4629A>G
NM_001271162.1:c.*4629A>G	NP_001258091.1:n.*4629A>G
NR_073141.2:n.7372A>G
NR_073142.2:n.7255A>G
NR_073143.2:n.6987A>G
NM_001271162.2:c.*4629A>G	NP_001258091.1:n.*4629A>G
NR_073141.3:n.7386A>G
NR_073142.3:n.7269A>G
NR_073143.3:n.7001A>G