Canonical Allele Identifier: CA356791698
Community Standard Title: NM_001080476.3(GRXCR1):c.696A>T (p.Arg232Ser)
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_001080476.3:c.696A>T MANE Select NP_001073945.1:p.Arg232Ser
ENST00000399770.3:c.696A>T MANE Select ENSP00000382670.2:p.Arg232Ser
NM_001080476.2:c.696A>T NP_001073945.1:p.Arg232Ser
ENST00000399770.2:c.696A>T ENSP00000382670.2:p.Arg232Ser
XM_011513691.1:c.333A>T XP_011511993.1:p.Arg111Ser