Canonical Allele Identifier: CA356792213
Gene: GRXCR1 HGNC NCBI

Linked Data

COSMIC: COSM4600184
MyVariant Identifiers: chr4:g.42964969G>T (hg19) chr4:g.42962952G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962952G>T , CM000666.2:g.42962952G>T GRCh38
NC_000004.11:g.42964969G>T , CM000666.1:g.42964969G>T GRCh37
NC_000004.10:g.42659726G>T NCBI36
NG_027718.1:g.74687G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.445G>T MANE Select ENSP00000382670.2:p.Val149Phe
ENST00000399770.2:c.445G>T ENSP00000382670.2:p.Val149Phe
NM_001080476.2:c.445G>T NP_001073945.1:p.Val149Phe
XM_011513691.1:c.82G>T XP_011511993.1:p.Val28Phe
NM_001080476.3:c.445G>T MANE Select NP_001073945.1:p.Val149Phe
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