Canonical Allele Identifier: CA356792298
Gene: GRXCR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962995T>G , CM000666.2:g.42962995T>G GRCh38
NC_000004.11:g.42965012T>G , CM000666.1:g.42965012T>G GRCh37
NC_000004.10:g.42659769T>G NCBI36
NG_027718.1:g.74730T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.488T>G MANE Select ENSP00000382670.2:p.Phe163Cys
ENST00000399770.2:c.488T>G ENSP00000382670.2:p.Phe163Cys
NM_001080476.2:c.488T>G NP_001073945.1:p.Phe163Cys
XM_011513691.1:c.125T>G XP_011511993.1:p.Phe42Cys
NM_001080476.3:c.488T>G MANE Select NP_001073945.1:p.Phe163Cys