Canonical Allele Identifier: CA1453040342
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42893568G= , CM000666.2:g.42893568G= GRCh38
NC_000004.11:g.42895585G= , CM000666.1:g.42895585G= GRCh37
NC_000004.10:g.42590342G= NCBI36
NG_027718.1:g.5303G=

Transcript Alleles

HGVS Amino-acid change
ENST00000399770.3:c.302G= MANE Select ENSP00000382670.2:p.Ser101=
ENST00000399770.2:c.302G= ENSP00000382670.2:p.Ser101=
NM_001080476.2:c.302G= NP_001073945.1:p.Ser101=
NM_001080476.3:c.302G= MANE Select NP_001073945.1:p.Ser101=