Canonical Allele Identifier: CA1453040338
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42893555G= , CM000666.2:g.42893555G= GRCh38
NC_000004.11:g.42895572G= , CM000666.1:g.42895572G= GRCh37
NC_000004.10:g.42590329G= NCBI36
NG_027718.1:g.5290G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.289G= MANE Select ENSP00000382670.2:p.Val97=
ENST00000399770.2:c.289G= ENSP00000382670.2:p.Val97=
NM_001080476.2:c.289G= NP_001073945.1:p.Val97=
NM_001080476.3:c.289G= MANE Select NP_001073945.1:p.Val97=