Canonical Allele Identifier: CA439192086
Community Standard Title: NM_001080476.3(GRXCR1):c.696A>G (p.Arg232=)
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.43030363A>G , CM000666.2:g.43030363A>G GRCh38
NC_000004.11:g.43032380A>G , CM000666.1:g.43032380A>G GRCh37
NC_000004.10:g.42727137A>G NCBI36
NG_027718.1:g.142098A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001080476.3:c.696A>G MANE Select NP_001073945.1:p.Arg232=
ENST00000399770.3:c.696A>G MANE Select ENSP00000382670.2:p.Arg232=
NM_001080476.2:c.696A>G NP_001073945.1:p.Arg232=
ENST00000399770.2:c.696A>G ENSP00000382670.2:p.Arg232=
XM_011513691.1:c.333A>G XP_011511993.1:p.Arg111=