Canonical Allele Identifier: CA356792268
Gene: GRXCR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962980T>G , CM000666.2:g.42962980T>G GRCh38
NC_000004.11:g.42964997T>G , CM000666.1:g.42964997T>G GRCh37
NC_000004.10:g.42659754T>G NCBI36
NG_027718.1:g.74715T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.473T>G MANE Select ENSP00000382670.2:p.Leu158Arg
ENST00000399770.2:c.473T>G ENSP00000382670.2:p.Leu158Arg
NM_001080476.2:c.473T>G NP_001073945.1:p.Leu158Arg
XM_011513691.1:c.110T>G XP_011511993.1:p.Leu37Arg
NM_001080476.3:c.473T>G MANE Select NP_001073945.1:p.Leu158Arg