Canonical Allele Identifier: CA356791498
Gene: GRXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.42895582T>G (hg19) chr4:g.42893565T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42893565T>G , CM000666.2:g.42893565T>G GRCh38
NC_000004.11:g.42895582T>G , CM000666.1:g.42895582T>G GRCh37
NC_000004.10:g.42590339T>G NCBI36
NG_027718.1:g.5300T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000399770.3:c.299T>G MANE Select ENSP00000382670.2:p.Leu100Ter
ENST00000399770.2:c.299T>G ENSP00000382670.2:p.Leu100Ter
NM_001080476.2:c.299T>G NP_001073945.1:p.Leu100Ter
NM_001080476.3:c.299T>G MANE Select NP_001073945.1:p.Leu100Ter
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