Canonical Allele Identifier: CA439191648
Gene: GRXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.42965061T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42963044T>A , CM000666.2:g.42963044T>A GRCh38
NC_000004.11:g.42965061T>A , CM000666.1:g.42965061T>A GRCh37
NC_000004.10:g.42659818T>A NCBI36
NG_027718.1:g.74779T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.537T>A MANE Select ENSP00000382670.2:p.Gly179=
ENST00000399770.2:c.537T>A ENSP00000382670.2:p.Gly179=
NM_001080476.2:c.537T>A NP_001073945.1:p.Gly179=
XM_011513691.1:c.174T>A XP_011511993.1:p.Gly58=
NM_001080476.3:c.537T>A MANE Select NP_001073945.1:p.Gly179=
Search 100 bp 5'
Search 100 bp 3'