Canonical Allele Identifier: CA1453073780
Gene: GRXCR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963003C= , CM000666.2:g.42963003C= GRCh38
NC_000004.11:g.42965020C= , CM000666.1:g.42965020C= GRCh37
NC_000004.10:g.42659777C= NCBI36
NG_027718.1:g.74738C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.496C= MANE Select ENSP00000382670.2:p.His166=
ENST00000399770.2:c.496C= ENSP00000382670.2:p.His166=
NM_001080476.2:c.496C= NP_001073945.1:p.His166=
XM_011513691.1:c.133C= XP_011511993.1:p.His45=
NM_001080476.3:c.496C= MANE Select NP_001073945.1:p.His166=
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