Canonical Allele Identifier: CA356792136
Gene: GRXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.42964930T>G (hg19) chr4:g.42962913T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962913T>G , CM000666.2:g.42962913T>G GRCh38
NC_000004.11:g.42964930T>G , CM000666.1:g.42964930T>G GRCh37
NC_000004.10:g.42659687T>G NCBI36
NG_027718.1:g.74648T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.406T>G MANE Select ENSP00000382670.2:p.Phe136Val
ENST00000399770.2:c.406T>G ENSP00000382670.2:p.Phe136Val
NM_001080476.2:c.406T>G NP_001073945.1:p.Phe136Val
XM_011513691.1:c.43T>G XP_011511993.1:p.Phe15Val
NM_001080476.3:c.406T>G MANE Select NP_001073945.1:p.Phe136Val
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