Canonical Allele Identifier: CA356792394
Gene: GRXCR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963039A>T , CM000666.2:g.42963039A>T GRCh38
NC_000004.11:g.42965056A>T , CM000666.1:g.42965056A>T GRCh37
NC_000004.10:g.42659813A>T NCBI36
NG_027718.1:g.74774A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.532A>T MANE Select ENSP00000382670.2:p.Asn178Tyr
ENST00000399770.2:c.532A>T ENSP00000382670.2:p.Asn178Tyr
NM_001080476.2:c.532A>T NP_001073945.1:p.Asn178Tyr
XM_011513691.1:c.169A>T XP_011511993.1:p.Asn57Tyr
NM_001080476.3:c.532A>T MANE Select NP_001073945.1:p.Asn178Tyr