Canonical Allele Identifier: CA356792271
Gene: GRXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.42965000T>A (hg19) chr4:g.42962983T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962983T>A , CM000666.2:g.42962983T>A GRCh38
NC_000004.11:g.42965000T>A , CM000666.1:g.42965000T>A GRCh37
NC_000004.10:g.42659757T>A NCBI36
NG_027718.1:g.74718T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.476T>A MANE Select ENSP00000382670.2:p.Val159Asp
ENST00000399770.2:c.476T>A ENSP00000382670.2:p.Val159Asp
NM_001080476.2:c.476T>A NP_001073945.1:p.Val159Asp
XM_011513691.1:c.113T>A XP_011511993.1:p.Val38Asp
NM_001080476.3:c.476T>A MANE Select NP_001073945.1:p.Val159Asp
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