Canonical Allele Identifier: CA1453040341
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42893562T= , CM000666.2:g.42893562T= GRCh38
NC_000004.11:g.42895579T= , CM000666.1:g.42895579T= GRCh37
NC_000004.10:g.42590336T= NCBI36
NG_027718.1:g.5297T=

Transcript Alleles

HGVS Amino-acid change
ENST00000399770.3:c.296T= MANE Select ENSP00000382670.2:p.Ile99=
ENST00000399770.2:c.296T= ENSP00000382670.2:p.Ile99=
NM_001080476.2:c.296T= NP_001073945.1:p.Ile99=
NM_001080476.3:c.296T= MANE Select NP_001073945.1:p.Ile99=