Canonical Allele Identifier: CA356792228
Gene: GRXCR1 HGNC NCBI

Linked Data

gnomAD v4: 4-42962962-C-T
COSMIC: COSM733394
MyVariant Identifiers: chr4:g.42964979C>T (hg19) chr4:g.42962962C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962962C>T , CM000666.2:g.42962962C>T GRCh38
NC_000004.11:g.42964979C>T , CM000666.1:g.42964979C>T GRCh37
NC_000004.10:g.42659736C>T NCBI36
NG_027718.1:g.74697C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.455C>T MANE Select ENSP00000382670.2:p.Thr152Ile
ENST00000399770.2:c.455C>T ENSP00000382670.2:p.Thr152Ile
NM_001080476.2:c.455C>T NP_001073945.1:p.Thr152Ile
XM_011513691.1:c.92C>T XP_011511993.1:p.Thr31Ile
NM_001080476.3:c.455C>T MANE Select NP_001073945.1:p.Thr152Ile
Search 100 bp 5'
Search 100 bp 3'