Canonical Allele Identifier: CA1453073759
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962956G= , CM000666.2:g.42962956G= GRCh38
NC_000004.11:g.42964973G= , CM000666.1:g.42964973G= GRCh37
NC_000004.10:g.42659730G= NCBI36
NG_027718.1:g.74691G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.449G= MANE Select ENSP00000382670.2:p.Arg150=
ENST00000399770.2:c.449G= ENSP00000382670.2:p.Arg150=
NM_001080476.2:c.449G= NP_001073945.1:p.Arg150=
XM_011513691.1:c.86G= XP_011511993.1:p.Arg29=
NM_001080476.3:c.449G= MANE Select NP_001073945.1:p.Arg150=