Canonical Allele Identifier: CA356792278
Gene: GRXCR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962987A>C , CM000666.2:g.42962987A>C GRCh38
NC_000004.11:g.42965004A>C , CM000666.1:g.42965004A>C GRCh37
NC_000004.10:g.42659761A>C NCBI36
NG_027718.1:g.74722A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.480A>C MANE Select ENSP00000382670.2:p.Arg160Ser
ENST00000399770.2:c.480A>C ENSP00000382670.2:p.Arg160Ser
NM_001080476.2:c.480A>C NP_001073945.1:p.Arg160Ser
XM_011513691.1:c.117A>C XP_011511993.1:p.Arg39Ser
NM_001080476.3:c.480A>C MANE Select NP_001073945.1:p.Arg160Ser