Canonical Allele Identifier: CA439191844
Gene: GRXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.42895581T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42893564T>C , CM000666.2:g.42893564T>C GRCh38
NC_000004.11:g.42895581T>C , CM000666.1:g.42895581T>C GRCh37
NC_000004.10:g.42590338T>C NCBI36
NG_027718.1:g.5299T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000399770.3:c.298T>C MANE Select ENSP00000382670.2:p.Leu100=
ENST00000399770.2:c.298T>C ENSP00000382670.2:p.Leu100=
NM_001080476.2:c.298T>C NP_001073945.1:p.Leu100=
NM_001080476.3:c.298T>C MANE Select NP_001073945.1:p.Leu100=
Search 100 bp 5'
Search 100 bp 3'