Canonical Allele Identifier: CA356792371
Gene: GRXCR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963027A>G , CM000666.2:g.42963027A>G GRCh38
NC_000004.11:g.42965044A>G , CM000666.1:g.42965044A>G GRCh37
NC_000004.10:g.42659801A>G NCBI36
NG_027718.1:g.74762A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.520A>G MANE Select ENSP00000382670.2:p.Asn174Asp
ENST00000399770.2:c.520A>G ENSP00000382670.2:p.Asn174Asp
NM_001080476.2:c.520A>G NP_001073945.1:p.Asn174Asp
XM_011513691.1:c.157A>G XP_011511993.1:p.Asn53Asp
NM_001080476.3:c.520A>G MANE Select NP_001073945.1:p.Asn174Asp