Canonical Allele Identifier: CA439192087
Community Standard Title: NM_001080476.3(GRXCR1):c.699A>C (p.Val233=)
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.43030366A>C , CM000666.2:g.43030366A>C GRCh38
NC_000004.11:g.43032383A>C , CM000666.1:g.43032383A>C GRCh37
NC_000004.10:g.42727140A>C NCBI36
NG_027718.1:g.142101A>C

Transcript Alleles

HGVS Amino-acid Change
NM_001080476.3:c.699A>C MANE Select NP_001073945.1:p.Val233=
ENST00000399770.3:c.699A>C MANE Select ENSP00000382670.2:p.Val233=
NM_001080476.2:c.699A>C NP_001073945.1:p.Val233=
ENST00000399770.2:c.699A>C ENSP00000382670.2:p.Val233=
XM_011513691.1:c.336A>C XP_011511993.1:p.Val112=