Canonical Allele Identifier: CA439191547

Gene: GRXCR1

Linked Data

• MyVariant Identifiers: chr4:g.42964977A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42962960A>G , CM000666.2:g.42962960A>G	GRCh38
NC_000004.11:g.42964977A>G , CM000666.1:g.42964977A>G	GRCh37
NC_000004.10:g.42659734A>G	NCBI36
NG_027718.1:g.74695A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.453A>G MANE Select	ENSP00000382670.2:p.Thr151=
ENST00000399770.2:c.453A>G	ENSP00000382670.2:p.Thr151=
NM_001080476.2:c.453A>G	NP_001073945.1:p.Thr151=
XM_011513691.1:c.90A>G	XP_011511993.1:p.Thr30=
NM_001080476.3:c.453A>G MANE Select	NP_001073945.1:p.Thr151=