Canonical Allele Identifier: CA1453073969
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963355C= , CM000666.2:g.42963355C= GRCh38
NC_000004.11:g.42965372C= , CM000666.1:g.42965372C= GRCh37
NC_000004.10:g.42660129C= NCBI36
NG_027718.1:g.75090C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+221C= MANE Select ENSP00000382670.2:n.627+221C=
ENST00000399770.2:c.627+221C= ENSP00000382670.2:n.627+221C=
NM_001080476.2:c.627+221C= NP_001073945.1:n.627+221C=
XM_011513691.1:c.264+221C= XP_011511993.1:n.264+221C=
NM_001080476.3:c.627+221C= MANE Select NP_001073945.1:n.627+221C=