Canonical Allele Identifier: CA96311691
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs573476478
gnomAD v3: 4-42963206-T-C
gnomAD v4: 4-42963206-T-C
MyVariant Identifiers: chr4:g.42965223T>C (hg19) chr4:g.42963206T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963206T>C , CM000666.2:g.42963206T>C GRCh38
NC_000004.11:g.42965223T>C , CM000666.1:g.42965223T>C GRCh37
NC_000004.10:g.42659980T>C NCBI36
NG_027718.1:g.74941T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+72T>C MANE Select ENSP00000382670.2:n.627+72T>C
ENST00000399770.2:c.627+72T>C ENSP00000382670.2:n.627+72T>C
NM_001080476.2:c.627+72T>C NP_001073945.1:n.627+72T>C
XM_011513691.1:c.264+72T>C XP_011511993.1:n.264+72T>C
NM_001080476.3:c.627+72T>C MANE Select NP_001073945.1:n.627+72T>C
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