Canonical Allele Identifier: CA356791486
Gene: GRXCR1 HGNC NCBI

Linked Data

gnomAD v4: 4-42893560-C-A
MyVariant Identifiers: chr4:g.42895577C>A (hg19) chr4:g.42893560C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42893560C>A , CM000666.2:g.42893560C>A GRCh38
NC_000004.11:g.42895577C>A , CM000666.1:g.42895577C>A GRCh37
NC_000004.10:g.42590334C>A NCBI36
NG_027718.1:g.5295C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.294C>A MANE Select ENSP00000382670.2:p.Asn98Lys
ENST00000399770.2:c.294C>A ENSP00000382670.2:p.Asn98Lys
NM_001080476.2:c.294C>A NP_001073945.1:p.Asn98Lys
NM_001080476.3:c.294C>A MANE Select NP_001073945.1:p.Asn98Lys
Search 100 bp 5'
Search 100 bp 3'