Canonical Allele Identifier: CA382437155
Gene: PGR HGNC NCBI

Linked Data

dbSNP Id: rs1042838
gnomAD v2: 11-100933412-C-G
gnomAD v4: 11-101062681-C-G
MyVariant Identifiers: chr11:g.100933412C>G (hg19) chr11:g.101062681C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101062681C>G , CM000673.2:g.101062681C>G GRCh38
NC_000011.9:g.100933412C>G , CM000673.1:g.100933412C>G GRCh37
NC_000011.8:g.100438622C>G NCBI36
NG_016475.1:g.72133G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325455.10:c.1978G>C MANE Select ENSP00000325120.5:p.Val660Leu
ENST00000263463.9:c.1907-11113G>C ENSP00000263463.5:n.1907-11113G>C
ENST00000325455.9:c.1978G>C ENSP00000325120.5:p.Val660Leu
ENST00000526300.5:c.1907-11113G>C ENSP00000436803.1:n.1907-11113G>C
ENST00000528960.5:c.1861G>C ENSP00000432914.1:p.Val621Leu
ENST00000533207.5:n.1345G>C
ENST00000534013.5:c.196G>C ENSP00000436561.1:p.Val66Leu
ENST00000534780.5:c.1978G>C ENSP00000432352.1:p.Val660Leu
ENST00000617858.4:c.1907-11113G>C ENSP00000481227.1:n.1907-11113G>C
ENST00000619228.2:c.1861G>C ENSP00000482698.1:p.Val621Leu
ENST00000632634.1:c.400G>C ENSP00000487607.1:p.Val134Leu
NM_000926.4:c.1978G>C MANE Select NP_000917.3:p.Val660Leu
NM_001202474.3:c.1486G>C NP_001189403.1:p.Val496Leu
NM_001271161.2:c.1415-11113G>C NP_001258090.1:n.1415-11113G>C
NM_001271162.1:c.196G>C NP_001258091.1:p.Val66Leu
NR_073141.2:n.1971G>C
NR_073142.2:n.1854G>C
NR_073143.2:n.1900-11113G>C
XM_006718858.2:c.1978G>C XP_006718921.1:p.Val660Leu
XR_947831.1:n.3550G>C
XM_006718858.3:c.1978G>C XP_006718921.1:p.Val660Leu
NM_001271162.2:c.196G>C NP_001258091.1:p.Val66Leu
NR_073141.3:n.1985G>C
NR_073142.3:n.1868G>C
NR_073143.3:n.1914-11113G>C
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