Canonical Allele Identifier: CA439191658

Gene: GRXCR1

Linked Data

• MyVariant Identifiers: chr4:g.42965070A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42963053A>T , CM000666.2:g.42963053A>T	GRCh38
NC_000004.11:g.42965070A>T , CM000666.1:g.42965070A>T	GRCh37
NC_000004.10:g.42659827A>T	NCBI36
NG_027718.1:g.74788A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.546A>T MANE Select	ENSP00000382670.2:p.Gly182=
ENST00000399770.2:c.546A>T	ENSP00000382670.2:p.Gly182=
NM_001080476.2:c.546A>T	NP_001073945.1:p.Gly182=
XM_011513691.1:c.183A>T	XP_011511993.1:p.Gly61=
NM_001080476.3:c.546A>T MANE Select	NP_001073945.1:p.Gly182=