Canonical Allele Identifier: CA356792262
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1748159242
gnomAD v2: 4-42964995-A-C
gnomAD v3: 4-42962978-A-C
gnomAD v4: 4-42962978-A-C
MyVariant Identifiers: chr4:g.42964995A>C (hg19) chr4:g.42962978A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962978A>C , CM000666.2:g.42962978A>C GRCh38
NC_000004.11:g.42964995A>C , CM000666.1:g.42964995A>C GRCh37
NC_000004.10:g.42659752A>C NCBI36
NG_027718.1:g.74713A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.471A>C MANE Select ENSP00000382670.2:p.Glu157Asp
ENST00000399770.2:c.471A>C ENSP00000382670.2:p.Glu157Asp
NM_001080476.2:c.471A>C NP_001073945.1:p.Glu157Asp
XM_011513691.1:c.108A>C XP_011511993.1:p.Glu36Asp
NM_001080476.3:c.471A>C MANE Select NP_001073945.1:p.Glu157Asp
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