Canonical Allele Identifier: CA439191596
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1748160321
MyVariant Identifiers: chr4:g.42965022T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963005T>C , CM000666.2:g.42963005T>C GRCh38
NC_000004.11:g.42965022T>C , CM000666.1:g.42965022T>C GRCh37
NC_000004.10:g.42659779T>C NCBI36
NG_027718.1:g.74740T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.498T>C MANE Select ENSP00000382670.2:p.His166=
ENST00000399770.2:c.498T>C ENSP00000382670.2:p.His166=
NM_001080476.2:c.498T>C NP_001073945.1:p.His166=
XM_011513691.1:c.135T>C XP_011511993.1:p.His45=
NM_001080476.3:c.498T>C MANE Select NP_001073945.1:p.His166=
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