Canonical Allele Identifier: CA439191545
Gene: GRXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.42964974G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962957G>T , CM000666.2:g.42962957G>T GRCh38
NC_000004.11:g.42964974G>T , CM000666.1:g.42964974G>T GRCh37
NC_000004.10:g.42659731G>T NCBI36
NG_027718.1:g.74692G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.450G>T MANE Select ENSP00000382670.2:p.Arg150=
ENST00000399770.2:c.450G>T ENSP00000382670.2:p.Arg150=
NM_001080476.2:c.450G>T NP_001073945.1:p.Arg150=
XM_011513691.1:c.87G>T XP_011511993.1:p.Arg29=
NM_001080476.3:c.450G>T MANE Select NP_001073945.1:p.Arg150=
Search 100 bp 5'
Search 100 bp 3'