Canonical Allele Identifier: CA439192176
Gene: GRXCR1 HGNC NCBI

Linked Data

gnomAD v4: 4-43030531-T-C
MyVariant Identifiers: chr4:g.43032548T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.43030531T>C , CM000666.2:g.43030531T>C GRCh38
NC_000004.11:g.43032548T>C , CM000666.1:g.43032548T>C GRCh37
NC_000004.10:g.42727305T>C NCBI36
NG_027718.1:g.142266T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000399770.3:c.864T>C MANE Select ENSP00000382670.2:p.Cys288=
ENST00000399770.2:c.864T>C ENSP00000382670.2:p.Cys288=
NM_001080476.2:c.864T>C NP_001073945.1:p.Cys288=
XM_011513691.1:c.501T>C XP_011511993.1:p.Cys167=
NM_001080476.3:c.864T>C MANE Select NP_001073945.1:p.Cys288=
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