Canonical Allele Identifier: CA2615658405
Gene: PGR HGNC NCBI

Linked Data

gnomAD v4: 11-101034526-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101034526T>C , CM000673.2:g.101034526T>C GRCh38
NC_000011.9:g.100905257T>C , CM000673.1:g.100905257T>C GRCh37
NC_000011.8:g.100410467T>C NCBI36
NG_016475.1:g.100288A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000325455.10:c.*4590A>G MANE Select ENSP00000325120.5:n.*4590A>G
ENST00000325455.9:c.*4590A>G ENSP00000325120.5:n.*4590A>G
NM_000926.4:c.*4590A>G MANE Select NP_000917.3:n.*4590A>G
NM_001202474.3:c.*4590A>G NP_001189403.1:n.*4590A>G
NM_001271161.2:c.*4590A>G NP_001258090.1:n.*4590A>G
NM_001271162.1:c.*4590A>G NP_001258091.1:n.*4590A>G
NR_073141.2:n.7333A>G
NR_073142.2:n.7216A>G
NR_073143.2:n.6948A>G
NM_001271162.2:c.*4590A>G NP_001258091.1:n.*4590A>G
NR_073141.3:n.7347A>G
NR_073142.3:n.7230A>G
NR_073143.3:n.6962A>G
Search 100 bp 5'
Search 100 bp 3'