Canonical Allele Identifier: CA356792336
Gene: GRXCR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963013A>G , CM000666.2:g.42963013A>G GRCh38
NC_000004.11:g.42965030A>G , CM000666.1:g.42965030A>G GRCh37
NC_000004.10:g.42659787A>G NCBI36
NG_027718.1:g.74748A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.506A>G MANE Select ENSP00000382670.2:p.Lys169Arg
ENST00000399770.2:c.506A>G ENSP00000382670.2:p.Lys169Arg
NM_001080476.2:c.506A>G NP_001073945.1:p.Lys169Arg
XM_011513691.1:c.143A>G XP_011511993.1:p.Lys48Arg
NM_001080476.3:c.506A>G MANE Select NP_001073945.1:p.Lys169Arg