Canonical Allele Identifier: CA439191510
Gene: GRXCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.42964953C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962936C>T , CM000666.2:g.42962936C>T GRCh38
NC_000004.11:g.42964953C>T , CM000666.1:g.42964953C>T GRCh37
NC_000004.10:g.42659710C>T NCBI36
NG_027718.1:g.74671C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.429C>T MANE Select ENSP00000382670.2:p.Thr143=
ENST00000399770.2:c.429C>T ENSP00000382670.2:p.Thr143=
NM_001080476.2:c.429C>T NP_001073945.1:p.Thr143=
XM_011513691.1:c.66C>T XP_011511993.1:p.Thr22=
NM_001080476.3:c.429C>T MANE Select NP_001073945.1:p.Thr143=
Search 100 bp 5'
Search 100 bp 3'