Canonical Allele Identifier: CA439191539
Gene: GRXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.42964972C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962955C>A , CM000666.2:g.42962955C>A GRCh38
NC_000004.11:g.42964972C>A , CM000666.1:g.42964972C>A GRCh37
NC_000004.10:g.42659729C>A NCBI36
NG_027718.1:g.74690C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.448C>A MANE Select ENSP00000382670.2:p.Arg150=
ENST00000399770.2:c.448C>A ENSP00000382670.2:p.Arg150=
NM_001080476.2:c.448C>A NP_001073945.1:p.Arg150=
XM_011513691.1:c.85C>A XP_011511993.1:p.Arg29=
NM_001080476.3:c.448C>A MANE Select NP_001073945.1:p.Arg150=
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