Canonical Allele Identifier: CA439191517
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs2109774961
MyVariant Identifiers: chr4:g.42964956C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962939C>G , CM000666.2:g.42962939C>G GRCh38
NC_000004.11:g.42964956C>G , CM000666.1:g.42964956C>G GRCh37
NC_000004.10:g.42659713C>G NCBI36
NG_027718.1:g.74674C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.432C>G MANE Select ENSP00000382670.2:p.Thr144=
ENST00000399770.2:c.432C>G ENSP00000382670.2:p.Thr144=
NM_001080476.2:c.432C>G NP_001073945.1:p.Thr144=
XM_011513691.1:c.69C>G XP_011511993.1:p.Thr23=
NM_001080476.3:c.432C>G MANE Select NP_001073945.1:p.Thr144=
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