Canonical Allele Identifier: CA356792086
Gene: GRXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.43032557A>C (hg19) chr4:g.43030540A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.43030540A>C , CM000666.2:g.43030540A>C GRCh38
NC_000004.11:g.43032557A>C , CM000666.1:g.43032557A>C GRCh37
NC_000004.10:g.42727314A>C NCBI36
NG_027718.1:g.142275A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000399770.3:c.873A>C MANE Select ENSP00000382670.2:p.Ter291Tyr
ENST00000399770.2:c.873A>C ENSP00000382670.2:p.Ter291Tyr
NM_001080476.2:c.873A>C NP_001073945.1:p.Ter291Tyr
XM_011513691.1:c.510A>C XP_011511993.1:p.Ter170Tyr
NM_001080476.3:c.873A>C MANE Select NP_001073945.1:p.Ter291Tyr
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