Canonical Allele Identifier: CA1924469957
Gene: RGR HGNC NCBI

Linked Data

dbSNP Id: rs1842761084

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.84247516T>C , CM000672.2:g.84247516T>C GRCh38
NC_000010.10:g.86007272T>C , CM000672.1:g.86007272T>C GRCh37
NC_000010.9:g.85997252T>C NCBI36
NG_009106.1:g.7464T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358110.7:c.80-75T>C ENSP00000350823.5:n.80-75T>C
ENST00000359452.9:c.80-75T>C ENSP00000352427.4:n.80-75T>C
ENST00000478727.6:c.*76T>C ENSP00000498966.1:n.*76T>C
ENST00000483744.6:c.80-75T>C ENSP00000498992.1:n.80-75T>C
ENST00000650682.1:c.-533T>C ENSP00000498223.1:n.-533T>C
ENST00000650774.1:c.80-125T>C ENSP00000498908.1:n.80-125T>C
ENST00000651155.1:c.80-75T>C ENSP00000499193.1:n.80-75T>C
ENST00000651237.1:c.-533T>C ENSP00000498404.1:n.-533T>C
ENST00000652073.1:c.-458-75T>C ENSP00000498800.1:n.-458-75T>C
ENST00000652092.2:c.80-75T>C MANE Select ENSP00000498299.1:n.80-75T>C
ENST00000652122.1:c.80-75T>C ENSP00000498917.1:n.80-75T>C
ENST00000652310.1:c.*58-125T>C ENSP00000498927.1:n.*58-125T>C
ENST00000358110.6:c.80-75T>C ENSP00000350823.5:n.80-75T>C
ENST00000359452.8:c.80-75T>C ENSP00000352427.4:n.80-75T>C
ENST00000372092.3:c.80-125T>C ENSP00000361164.3:n.80-125T>C
ENST00000469446.5:n.118-75T>C
ENST00000478727.5:n.118-75T>C
ENST00000483660.5:n.108-1406T>C
ENST00000483771.5:n.82-125T>C
NM_001012720.1:c.80-75T>C NP_001012738.1:n.80-75T>C
NM_001012722.1:c.80-75T>C NP_001012740.1:n.80-75T>C
NM_002921.3:c.80-75T>C NP_002912.2:n.80-75T>C
XM_011540028.1:c.107-75T>C XP_011538330.1:n.107-75T>C
XM_024448118.1:c.80-75T>C XP_024303886.1:n.80-75T>C
XR_002957005.1:n.1430-75T>C
NM_001012720.2:c.80-75T>C MANE Select NP_001012738.1:n.80-75T>C
NM_001012722.2:c.80-75T>C NP_001012740.1:n.80-75T>C
NM_002921.4:c.80-75T>C NP_002912.2:n.80-75T>C