Canonical Allele Identifier: CA1453040340
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.294C= MANE Select ENSP00000382670.2:p.Asn98=
ENST00000399770.2:c.294C= ENSP00000382670.2:p.Asn98=
NM_001080476.2:c.294C= NP_001073945.1:p.Asn98=
NM_001080476.3:c.294C= MANE Select NP_001073945.1:p.Asn98=