Canonical Allele Identifier: CA377390865
Gene: RGR HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.86007465C>G (hg19) chr10:g.84247709C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.84247709C>G , CM000672.2:g.84247709C>G GRCh38
NC_000010.10:g.86007465C>G , CM000672.1:g.86007465C>G GRCh37
NC_000010.9:g.85997445C>G NCBI36
NG_009106.1:g.7657C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000358110.7:c.198C>G ENSP00000350823.5:p.Ser66Arg
ENST00000359452.9:c.198C>G ENSP00000352427.4:p.Ser66Arg
ENST00000478727.6:c.*269C>G ENSP00000498966.1:n.*269C>G
ENST00000483744.6:c.198C>G ENSP00000498992.1:p.Ser66Arg
ENST00000650682.1:c.-340C>G ENSP00000498223.1:n.-340C>G
ENST00000650774.1:c.148C>G ENSP00000498908.1:p.Pro50Ala
ENST00000651155.1:c.198C>G ENSP00000499193.1:p.Ser66Arg
ENST00000651237.1:c.-340C>G ENSP00000498404.1:n.-340C>G
ENST00000652073.1:c.-340C>G ENSP00000498800.1:n.-340C>G
ENST00000652092.2:c.198C>G MANE Select ENSP00000498299.1:p.Ser66Arg
ENST00000652122.1:c.198C>G ENSP00000498917.1:p.Ser66Arg
ENST00000652310.1:c.*126C>G ENSP00000498927.1:n.*126C>G
ENST00000358110.6:c.198C>G ENSP00000350823.5:p.Ser66Arg
ENST00000359452.8:c.198C>G ENSP00000352427.4:p.Ser66Arg
ENST00000372092.3:c.148C>G ENSP00000361164.3:p.Pro50Ala
ENST00000469446.5:n.236C>G
ENST00000478727.5:n.236C>G
ENST00000483660.5:n.108-1213C>G
ENST00000483744.5:n.5C>G
ENST00000483771.5:n.150C>G
NM_001012720.1:c.198C>G NP_001012738.1:p.Ser66Arg
NM_001012722.1:c.198C>G NP_001012740.1:p.Ser66Arg
NM_002921.3:c.198C>G NP_002912.2:p.Ser66Arg
XM_011540028.1:c.225C>G XP_011538330.1:p.Ser75Arg
XM_024448118.1:c.198C>G XP_024303886.1:p.Ser66Arg
XR_002957005.1:n.1548C>G
NM_001012720.2:c.198C>G MANE Select NP_001012738.1:p.Ser66Arg
NM_001012722.2:c.198C>G NP_001012740.1:p.Ser66Arg
NM_002921.4:c.198C>G NP_002912.2:p.Ser66Arg
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