Canonical Allele Identifier: CA670697101

Gene: PGR

Linked Data

• dbSNP Id: rs1417826170
• MyVariant Identifiers: chr11:g.100905355A>C (hg19) ; chr11:g.101034624A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034624A>C , CM000673.2:g.101034624A>C	GRCh38
NC_000011.9:g.100905355A>C , CM000673.1:g.100905355A>C	GRCh37
NC_000011.8:g.100410565A>C	NCBI36
NG_016475.1:g.100190T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4492T>G MANE Select	ENSP00000325120.5:n.*4492T>G
ENST00000325455.9:c.*4492T>G	ENSP00000325120.5:n.*4492T>G
NM_000926.4:c.*4492T>G MANE Select	NP_000917.3:n.*4492T>G
NM_001202474.3:c.*4492T>G	NP_001189403.1:n.*4492T>G
NM_001271161.2:c.*4492T>G	NP_001258090.1:n.*4492T>G
NM_001271162.1:c.*4492T>G	NP_001258091.1:n.*4492T>G
NR_073141.2:n.7235T>G
NR_073142.2:n.7118T>G
NR_073143.2:n.6850T>G
NM_001271162.2:c.*4492T>G	NP_001258091.1:n.*4492T>G
NR_073141.3:n.7249T>G
NR_073142.3:n.7132T>G
NR_073143.3:n.6864T>G