Canonical Allele Identifier: CA1453107620
Community Standard Title: NM_001080476.3(GRXCR1):c.698T= (p.Val233=)
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.43030365T= , CM000666.2:g.43030365T= GRCh38
NC_000004.11:g.43032382T= , CM000666.1:g.43032382T= GRCh37
NC_000004.10:g.42727139T= NCBI36
NG_027718.1:g.142100T=

Transcript Alleles

HGVS Amino-acid Change
NM_001080476.3:c.698T= MANE Select NP_001073945.1:p.Val233=
ENST00000399770.3:c.698T= MANE Select ENSP00000382670.2:p.Val233=
NM_001080476.2:c.698T= NP_001073945.1:p.Val233=
ENST00000399770.2:c.698T= ENSP00000382670.2:p.Val233=
XM_011513691.1:c.335T= XP_011511993.1:p.Val112=