Canonical Allele Identifier: CA1453073760
Gene: GRXCR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962958A= , CM000666.2:g.42962958A= GRCh38
NC_000004.11:g.42964975A= , CM000666.1:g.42964975A= GRCh37
NC_000004.10:g.42659732A= NCBI36
NG_027718.1:g.74693A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.451A= MANE Select ENSP00000382670.2:p.Thr151=
ENST00000399770.2:c.451A= ENSP00000382670.2:p.Thr151=
NM_001080476.2:c.451A= NP_001073945.1:p.Thr151=
XM_011513691.1:c.88A= XP_011511993.1:p.Thr30=
NM_001080476.3:c.451A= MANE Select NP_001073945.1:p.Thr151=
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