Canonical Allele Identifier: CA356792082
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1713394785
MyVariant Identifiers: chr4:g.43032555T>C (hg19) chr4:g.43030538T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.43030538T>C , CM000666.2:g.43030538T>C GRCh38
NC_000004.11:g.43032555T>C , CM000666.1:g.43032555T>C GRCh37
NC_000004.10:g.42727312T>C NCBI36
NG_027718.1:g.142273T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000399770.3:c.871T>C MANE Select ENSP00000382670.2:p.Ter291Gln
ENST00000399770.2:c.871T>C ENSP00000382670.2:p.Ter291Gln
NM_001080476.2:c.871T>C NP_001073945.1:p.Ter291Gln
XM_011513691.1:c.508T>C XP_011511993.1:p.Ter170Gln
NM_001080476.3:c.871T>C MANE Select NP_001073945.1:p.Ter291Gln
Search 100 bp 5'
Search 100 bp 3'