Canonical Allele Identifier: CA439191620
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1347688069
gnomAD v4: 4-42963023-G-A
MyVariant Identifiers: chr4:g.42965040G>A (hg19) chr4:g.42963023G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963023G>A , CM000666.2:g.42963023G>A GRCh38
NC_000004.11:g.42965040G>A , CM000666.1:g.42965040G>A GRCh37
NC_000004.10:g.42659797G>A NCBI36
NG_027718.1:g.74758G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.516G>A MANE Select ENSP00000382670.2:p.Glu172=
ENST00000399770.2:c.516G>A ENSP00000382670.2:p.Glu172=
NM_001080476.2:c.516G>A NP_001073945.1:p.Glu172=
XM_011513691.1:c.153G>A XP_011511993.1:p.Glu51=
NM_001080476.3:c.516G>A MANE Select NP_001073945.1:p.Glu172=
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