Canonical Allele Identifier: CA356792338
Gene: GRXCR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2302878
ClinVar RCV Id: RCV002886990
MyVariant Identifiers: chr4:g.42965031A>T (hg19) chr4:g.42963014A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963014A>T , CM000666.2:g.42963014A>T GRCh38
NC_000004.11:g.42965031A>T , CM000666.1:g.42965031A>T GRCh37
NC_000004.10:g.42659788A>T NCBI36
NG_027718.1:g.74749A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.507A>T MANE Select ENSP00000382670.2:p.Lys169Asn
ENST00000399770.2:c.507A>T ENSP00000382670.2:p.Lys169Asn
NM_001080476.2:c.507A>T NP_001073945.1:p.Lys169Asn
XM_011513691.1:c.144A>T XP_011511993.1:p.Lys48Asn
NM_001080476.3:c.507A>T MANE Select NP_001073945.1:p.Lys169Asn
Search 100 bp 5'
Search 100 bp 3'