Canonical Allele Identifier: CA439191647

Gene: GRXCR1

Linked Data

• MyVariant Identifiers: chr4:g.42965061T>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.537T>G MANE Select	ENSP00000382670.2:p.Gly179=
ENST00000399770.2:c.537T>G	ENSP00000382670.2:p.Gly179=
NM_001080476.2:c.537T>G	NP_001073945.1:p.Gly179=
XM_011513691.1:c.174T>G	XP_011511993.1:p.Gly58=
NM_001080476.3:c.537T>G MANE Select	NP_001073945.1:p.Gly179=