Canonical Allele Identifier: CA356792078
Gene: GRXCR1 HGNC NCBI

Linked Data

COSMIC: COSM3604023
MyVariant Identifiers: chr4:g.43032553G>A (hg19) chr4:g.43030536G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.43030536G>A , CM000666.2:g.43030536G>A GRCh38
NC_000004.11:g.43032553G>A , CM000666.1:g.43032553G>A GRCh37
NC_000004.10:g.42727310G>A NCBI36
NG_027718.1:g.142271G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000399770.3:c.869G>A MANE Select ENSP00000382670.2:p.Gly290Asp
ENST00000399770.2:c.869G>A ENSP00000382670.2:p.Gly290Asp
NM_001080476.2:c.869G>A NP_001073945.1:p.Gly290Asp
XM_011513691.1:c.506G>A XP_011511993.1:p.Gly169Asp
NM_001080476.3:c.869G>A MANE Select NP_001073945.1:p.Gly290Asp
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