Canonical Allele Identifier: CA1453073929
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963257A= , CM000666.2:g.42963257A= GRCh38
NC_000004.11:g.42965274A= , CM000666.1:g.42965274A= GRCh37
NC_000004.10:g.42660031A= NCBI36
NG_027718.1:g.74992A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.627+123A= MANE Select ENSP00000382670.2:n.627+123A=
ENST00000399770.2:c.627+123A= ENSP00000382670.2:n.627+123A=
NM_001080476.2:c.627+123A= NP_001073945.1:n.627+123A=
XM_011513691.1:c.264+123A= XP_011511993.1:n.264+123A=
NM_001080476.3:c.627+123A= MANE Select NP_001073945.1:n.627+123A=