Canonical Allele Identifier: CA2615658341
Gene: PGR HGNC NCBI

Linked Data

gnomAD v4: 11-101034388-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101034388T>C , CM000673.2:g.101034388T>C GRCh38
NC_000011.9:g.100905119T>C , CM000673.1:g.100905119T>C GRCh37
NC_000011.8:g.100410329T>C NCBI36
NG_016475.1:g.100426A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.*4728A>G MANE Select ENSP00000325120.5:n.*4728A>G
ENST00000325455.9:c.*4728A>G ENSP00000325120.5:n.*4728A>G
NM_000926.4:c.*4728A>G MANE Select NP_000917.3:n.*4728A>G
NM_001202474.3:c.*4728A>G NP_001189403.1:n.*4728A>G
NM_001271161.2:c.*4728A>G NP_001258090.1:n.*4728A>G
NM_001271162.1:c.*4728A>G NP_001258091.1:n.*4728A>G
NR_073141.2:n.7471A>G
NR_073142.2:n.7354A>G
NR_073143.2:n.7086A>G
NM_001271162.2:c.*4728A>G NP_001258091.1:n.*4728A>G
NR_073141.3:n.7485A>G
NR_073142.3:n.7368A>G
NR_073143.3:n.7100A>G
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