Canonical Allele Identifier: CA1924469968
Gene: RGR HGNC NCBI

Linked Data

dbSNP Id: rs1842761356

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.84247533G>C , CM000672.2:g.84247533G>C GRCh38
NC_000010.10:g.86007289G>C , CM000672.1:g.86007289G>C GRCh37
NC_000010.9:g.85997269G>C NCBI36
NG_009106.1:g.7481G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000358110.7:c.80-58G>C ENSP00000350823.5:n.80-58G>C
ENST00000359452.9:c.80-58G>C ENSP00000352427.4:n.80-58G>C
ENST00000478727.6:c.*93G>C ENSP00000498966.1:n.*93G>C
ENST00000483744.6:c.80-58G>C ENSP00000498992.1:n.80-58G>C
ENST00000650682.1:c.-516G>C ENSP00000498223.1:n.-516G>C
ENST00000650774.1:c.80-108G>C ENSP00000498908.1:n.80-108G>C
ENST00000651155.1:c.80-58G>C ENSP00000499193.1:n.80-58G>C
ENST00000651237.1:c.-516G>C ENSP00000498404.1:n.-516G>C
ENST00000652073.1:c.-458-58G>C ENSP00000498800.1:n.-458-58G>C
ENST00000652092.2:c.80-58G>C MANE Select ENSP00000498299.1:n.80-58G>C
ENST00000652122.1:c.80-58G>C ENSP00000498917.1:n.80-58G>C
ENST00000652310.1:c.*58-108G>C ENSP00000498927.1:n.*58-108G>C
ENST00000358110.6:c.80-58G>C ENSP00000350823.5:n.80-58G>C
ENST00000359452.8:c.80-58G>C ENSP00000352427.4:n.80-58G>C
ENST00000372092.3:c.80-108G>C ENSP00000361164.3:n.80-108G>C
ENST00000469446.5:n.118-58G>C
ENST00000478727.5:n.118-58G>C
ENST00000483660.5:n.108-1389G>C
ENST00000483771.5:n.82-108G>C
NM_001012720.1:c.80-58G>C NP_001012738.1:n.80-58G>C
NM_001012722.1:c.80-58G>C NP_001012740.1:n.80-58G>C
NM_002921.3:c.80-58G>C NP_002912.2:n.80-58G>C
XM_011540028.1:c.107-58G>C XP_011538330.1:n.107-58G>C
XM_024448118.1:c.80-58G>C XP_024303886.1:n.80-58G>C
XR_002957005.1:n.1430-58G>C
NM_001012720.2:c.80-58G>C MANE Select NP_001012738.1:n.80-58G>C
NM_001012722.2:c.80-58G>C NP_001012740.1:n.80-58G>C
NM_002921.4:c.80-58G>C NP_002912.2:n.80-58G>C