Canonical Allele Identifier: CA356792287

Gene: GRXCR1

Linked Data

• MyVariant Identifiers: chr4:g.42965008A>G (hg19) ; chr4:g.42962991A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42962991A>G , CM000666.2:g.42962991A>G	GRCh38
NC_000004.11:g.42965008A>G , CM000666.1:g.42965008A>G	GRCh37
NC_000004.10:g.42659765A>G	NCBI36
NG_027718.1:g.74726A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.484A>G MANE Select	ENSP00000382670.2:p.Ile162Val
ENST00000399770.2:c.484A>G	ENSP00000382670.2:p.Ile162Val
NM_001080476.2:c.484A>G	NP_001073945.1:p.Ile162Val
XM_011513691.1:c.121A>G	XP_011511993.1:p.Ile41Val
NM_001080476.3:c.484A>G MANE Select	NP_001073945.1:p.Ile162Val