Canonical Allele Identifier: CA439191603

Gene: GRXCR1

Linked Data

• MyVariant Identifiers: chr4:g.42965028A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42963011A>T , CM000666.2:g.42963011A>T	GRCh38
NC_000004.11:g.42965028A>T , CM000666.1:g.42965028A>T	GRCh37
NC_000004.10:g.42659785A>T	NCBI36
NG_027718.1:g.74746A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.504A>T MANE Select	ENSP00000382670.2:p.Val168=
ENST00000399770.2:c.504A>T	ENSP00000382670.2:p.Val168=
NM_001080476.2:c.504A>T	NP_001073945.1:p.Val168=
XM_011513691.1:c.141A>T	XP_011511993.1:p.Val47=
NM_001080476.3:c.504A>T MANE Select	NP_001073945.1:p.Val168=